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 2 exons, is associated with 2215 variant alleles and maps to 62 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: 2, Coding exons: 0, Transcript length: 660 bps,

Transcript Support Level (TSL)

TSL:2

Version

ENST00000423054.1

Type

Protein coding CDS not defined

Annotation Method

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