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Human (GRCh38.p14)
Description

retinoid isomerohydrolase RPE65 [Source:HGNC Symbol;Acc:HGNC:10294]

Gene Synonyms

BCO3, LCA2, RD12, RP20

Location
About this transcript

This transcript has 14 exons, is annotated with 4 domains and features, is associated with 9817 variant alleles and maps to 515 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000262340.6RPE65-2012605533aaENSP00000262340.5
 
Protein coding
CCDS643Q16518 NM_000329.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000713937.1RPE65-2034141412aaENSP00000519234.1
 
Nonsense mediated decay
---
ENST00000713936.1RPE65-202392086aaENSP00000519233.1
 
Nonsense mediated decay
---
ENST00000713938.1RPE65-2042306217aaENSP00000519235.1
 
Nonsense mediated decay
---
ENST00000713939.1RPE65-205209742aaENSP00000519236.1
 
Nonsense mediated decay
---
Statistics

Exons: 14, Coding exons: 14, Transcript length: 2,605 bps, Translation length: 533 residues

MANE

This MANE Select transcript contains ENSP00000262340 and matches to NM_000329.3 and NP_000320.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q16518

CCDS

This transcript is a member of the Human CCDS set: CCDS643

Transcript Support Level (TSL)

TSL:1

Version

ENST00000262340.6

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

GENCODE primary gene

This transcript is a member of the Gencode Primary gene set.