Human (GRCh38.p14)
Description

Bardet-Biedl syndrome 12 [Source:HGNC Symbol;Acc:HGNC:26648]

Gene Synonyms

C4ORF24, FLJ35630, FLJ41559

About this transcript

This transcript has 3 exons, is annotated with 10 domains and features, is associated with 5378 variant alleles and maps to 316 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000314218.8BBS12-2013238710aaENSP00000319062.3
 
Protein coding
CCDS3728Q6ZW61 NM_152618.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000542236.5BBS12-2033431710aaENSP00000438273.1
 
Protein coding
CCDS3728Q6ZW61 -GENCODE basicAPPRIS P1TSL:2
ENST00000433287.1BBS12-202859191aaENSP00000398912.1
 
Protein coding
C9J8H7 -TSL:2CDS 3' incomplete
Statistics

Exons: 3, Coding exons: 1, Transcript length: 3,431 bps, Translation length: 710 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q6ZW61

CCDS

This transcript is a member of the Human CCDS set: CCDS3728

Transcript Support Level (TSL)

TSL:2

Version

ENST00000542236.5

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.

GENCODE basic gene

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