We need your help! Has Ensembl saved you time or effort? Please take 15 minutes to fill in a survey and help EMBL-EBI make the case for why open data resources are critical to life science research.
https://www.surveymonkey.com/r/QGFMBH8?channel=[webpage]

Human (GRCh38.p14)
Description

Bardet-Biedl syndrome 5 [Source:HGNC Symbol;Acc:HGNC:970]

Gene Synonyms

DKFZP762I194

About this transcript

This transcript has 11 exons, is annotated with 7 domains and features, is associated with 12293 variant alleles and maps to 462 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000295240.8BBS5-2013159341aaENSP00000295240.3
 
Protein coding
CCDS2233Q8N3I7-1 NM_152384.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000392663.6BBS5-2023107320aaENSP00000376431.2
 
Protein coding
Q8N3I7-2 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000443151.1BBS5-20358353aaENSP00000406182.1
 
Nonsense mediated decay
F8WBR7 -TSL:5
ENST00000472667.1BBS5-2052705No protein-
 
Retained intron
--TSL:2
ENST00000469980.1BBS5-204593No protein-
 
Retained intron
--TSL:4
ENST00000475571.1BBS5-206566No protein-
 
Retained intron
--TSL:4
Statistics

Exons: 11, Coding exons: 11, Transcript length: 3,107 bps, Translation length: 320 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8N3I7

Transcript Support Level (TSL)

TSL:1

Version

ENST00000392663.6

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

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.