Human (GRCh38.p14)
Description

golgin A7 family member B [Source:HGNC Symbol;Acc:HGNC:31668]

Gene Synonyms

BA451M19.3, BA459F3.4, C10ORF132, C10ORF133

Location
About this transcript

This transcript has 5 exons, is annotated with 5 domains and features, is associated with 8744 variant alleles and maps to 432 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000370602.6GOLGA7B-2016843167aaENSP00000359634.1
 
Protein coding
CCDS31265Q2TAP0 NM_001010917.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000423054.1GOLGA7B-202660No protein-
 
Protein coding CDS not defined
--TSL:2
Statistics

Exons: 5, Coding exons: 5, Transcript length: 6,843 bps, Translation length: 167 residues

MANE

This MANE Select transcript contains ENSP00000359634 and matches to NM_001010917.3 and NP_001010917.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q2TAP0

CCDS

This transcript is a member of the Human CCDS set: CCDS31265

Transcript Support Level (TSL)

TSL:1

Version

ENST00000370602.6

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.