ensembl-rest-api

name	ensembl-rest-api
description	Query gene, sequence, and variant data via the Ensembl REST API
metadata	{"openclaw":{"emoji":"🧬","category":"domains","subcategory":"biomedical","keywords":["Ensembl","gene lookup","sequence retrieval","genomics","variant data","bioinformatics"],"source":"https://rest.ensembl.org"}}

Ensembl REST API Guide

Overview

Ensembl is a genome browser and annotation system maintained by EMBL-EBI and the Wellcome Sanger Institute, providing reference assemblies, gene annotations, variant data, and comparative genomics for over 300 vertebrate genomes. It is the genomic reference underpinning gget, PyEnsembl, and BioMart.

The REST API exposes Ensembl data via stateless HTTP. Researchers can look up genes by symbol or stable ID, retrieve genomic/cDNA/protein sequences, query variant annotations (rsIDs, clinical significance, consequences), access cross-references (HGNC, UniProt, RefSeq, OMIM), and obtain assembly metadata. Responses in JSON or XML.

Authentication

No authentication required. All endpoints are publicly accessible. Users needing higher throughput can register for an API token.

Core Endpoints

lookup/symbol: Gene Lookup by Symbol

Retrieve gene metadata: coordinates, biotype, canonical transcript.

• URL: GET https://rest.ensembl.org/lookup/symbol/{species}/{symbol}
• Parameters:

Parameter	Type	Required	Description
species	string	Yes	Species name (e.g., homo_sapiens)
symbol	string	Yes	Gene symbol (e.g., BRCA1, TP53)
expand	int	No	Set to 1 to include transcripts and translations
content-type	string	Yes	application/json or text/xml

• Example:

curl "https://rest.ensembl.org/lookup/symbol/homo_sapiens/BRCA1?content-type=application/json"

• Response (actual):

{
  "display_name": "BRCA1",
  "description": "BRCA1 DNA repair associated [Source:HGNC Symbol;Acc:HGNC:1100]",
  "object_type": "Gene", "species": "homo_sapiens",
  "assembly_name": "GRCh38", "biotype": "protein_coding",
  "seq_region_name": "17", "start": 43044292, "end": 43170245, "strand": -1,
  "id": "ENSG00000012048", "canonical_transcript": "ENST00000357654.9"
}

sequence/id: Sequence Retrieval

Retrieve genomic, cDNA, CDS, or protein sequences by Ensembl stable ID.

• URL: GET https://rest.ensembl.org/sequence/id/{id}
• Parameters:

Parameter	Type	Required	Description
id	string	Yes	Ensembl stable ID (e.g., ENSG00000012048)
type	string	No	genomic, cdna, cds, or protein
expand_5prime	int	No	Expand 5' flanking region by N bases
expand_3prime	int	No	Expand 3' flanking region by N bases
content-type	string	Yes	application/json or text/plain (FASTA)

• Example:

curl "https://rest.ensembl.org/sequence/id/ENSG00000012048?content-type=application/json&type=genomic"

• Response (actual, seq truncated):

{
  "id": "ENSG00000012048", "query": "ENSG00000012048",
  "desc": "chromosome:GRCh38:17:43044292:43170245:-1",
  "molecule": "DNA",
  "seq": "AAAGCGTGGGAATTACAGATAAATTAAAACTGTGGAACCCCTTTCCTCGGCTGCCGCCAAGGTGTTCGG..."
}

xrefs/symbol: Cross-References

Map a gene symbol to Ensembl stable IDs and external database identifiers.

• URL: GET https://rest.ensembl.org/xrefs/symbol/{species}/{symbol}
• Key params: species (required), symbol (required), external_db (optional filter, e.g., UniProt)
• Example:

curl "https://rest.ensembl.org/xrefs/symbol/homo_sapiens/TP53?content-type=application/json"

• Response (actual): [{"type":"gene","id":"ENSG00000141510"},{"type":"gene","id":"LRG_321"}]

Use xrefs/id/{id} to expand an Ensembl ID to all external cross-references (UniProt, HGNC, RefSeq, OMIM).

variation: Variant Annotation

Retrieve variant data by rsID: mappings, alleles, consequence, clinical significance.

• URL: GET https://rest.ensembl.org/variation/{species}/{id}
• Key params: species (required), id (required, e.g., rs699)
• Example:

curl "https://rest.ensembl.org/variation/homo_sapiens/rs699?content-type=application/json"

• Response (actual, synonyms truncated):

{
  "name": "rs699", "var_class": "SNP",
  "most_severe_consequence": "missense_variant",
  "clinical_significance": ["benign"],
  "evidence": ["Frequency","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"],
  "mappings": [{"location":"1:230710048-230710048","allele_string":"A/G","strand":1,"assembly_name":"GRCh38"}

info/assembly: Assembly Metadata

• URL: GET https://rest.ensembl.org/info/assembly/{species}
• Response (actual): Returns assembly_name ("GRCh38.p14"), assembly_date ("2013-12"), assembly_accession ("GCA_000001405.29"), full karyotype array (1-22, X, Y, MT), and 347 top_level_region entries.

Rate Limits

• Without token: 15 requests per second per IP.
• With token: higher limits available upon registration.
• Response headers: X-RateLimit-Limit, X-RateLimit-Remaining, X-RateLimit-Reset on every response.
• Batch POST endpoints (/lookup/id, /sequence/id): accept up to 1000 IDs per request.
• GRCh37 mirror: https://grch37.rest.ensembl.org

Academic Use Cases

• Gene annotation: Look up coordinates and biotypes for HGNC symbols to annotate RNA-seq results.
• Variant interpretation: Retrieve consequence types and clinical significance for GWAS rsIDs.
• ID mapping: Map between Ensembl, UniProt, RefSeq, and HGNC identifiers.
• Primer design: Fetch genomic sequences with flanking regions for PCR or CRISPR targeting.
• Comparative genomics: Query homology endpoints for orthologs across species.

Code Examples (Python)

Gene Lookup and Sequence Retrieval

import requests

BASE = "https://rest.ensembl.org"
HEADERS = {"Content-Type": "application/json"}

gene = requests.get(f"{BASE}/lookup/symbol/homo_sapiens/BRCA1", headers=HEADERS).json()
print(f"{gene['display_name']} ({gene['id']}) chr{gene['seq_region_name']}:{gene['start']}-{gene['end']}")

seq = requests.get(f"{BASE}/sequence/id/{gene['id']}?type=cds", headers=HEADERS).json()
print(f"CDS length: {len(seq['seq'])} bp")

Batch ID Lookup (POST)

import requests

ids = ["ENSG00000012048", "ENSG00000141510", "ENSG00000157764"]  # BRCA1, TP53, BRAF
resp = requests.post(
    "https://rest.ensembl.org/lookup/id",
    headers={"Content-Type": "application/json", "Accept": "application/json"},
    json={"ids": ids}
)
for ens_id, info in resp.json().items():
    print(f"{info['display_name']:10s} chr{info['seq_region_name']}:{info['start']}-{info['end']}")

Variant Annotation Pipeline

import requests

for rsid in ["rs699", "rs1042522", "rs334"]:
    v = requests.get(
        f"https://rest.ensembl.org/variation/homo_sapiens/{rsid}",
        headers={"Content-Type": "application/json"}
    ).json()
    loc = v["mappings"][0]["location"] if v.get("mappings") else "N/A"
    print(f"{v['name']:12s} {v['var_class']:5s} {v['most_severe_consequence']:25s} {loc}")

References

• REST API docs: https://rest.ensembl.org/documentation
• Ensembl browser: https://www.ensembl.org
• gget toolkit (built on Ensembl REST): https://pachterlab.github.io/gget/
• GRCh37 archive API: https://grch37.rest.ensembl.org