Human (GRCh38.p14)
Description

calcium binding protein 4 [Source:HGNC Symbol;Acc:HGNC:1386]

Gene Synonyms

CSNB2B

Location
About this transcript

This transcript has 6 exons, is annotated with 20 domains and features, is associated with 3308 variant alleles and maps to 351 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000325656.7CABP4-2013991275aaENSP00000324960.5
 
Protein coding
CCDS8166P57796-1 NM_145200.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000438189.6CABP4-2021426170aaENSP00000401555.2
 
Protein coding
CCDS73333P57796-2 -GENCODE basicTSL:1
ENST00000545777.1CABP4-207682128aaENSP00000439145.1
 
Nonsense mediated decay
F5H3E8 -TSL:3
ENST00000542025.2CABP4-204764No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000538060.1CABP4-203561No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000542233.1CABP4-205353No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000545040.1CABP4-206914No protein-
 
Retained intron
--TSL:1
Statistics

Exons: 6, Coding exons: 6, Transcript length: 3,991 bps, Translation length: 275 residues

MANE

This MANE Select transcript contains ENSP00000324960 and matches to NM_145200.5 and NP_660201.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P57796

CCDS

This transcript is a member of the Human CCDS set: CCDS8166

Transcript Support Level (TSL)

TSL:1

Version

ENST00000325656.7

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.