Human (GRCh38.p14)
Description

golgin A6 family member B [Source:HGNC Symbol;Acc:HGNC:32205]

Location
About this transcript

This transcript has 18 exons, is annotated with 22 domains and features, is associated with 6029 variant alleles and maps to 2762 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000421285.4GOLGA6B-2015380693aaENSP00000408132.3
 
Protein coding
CCDS10245A6NDN3 NM_018652.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000568532.1GOLGA6B-202402No protein-
 
Retained intron
--TSL:5
Statistics

Exons: 18, Coding exons: 18, Transcript length: 5,380 bps, Translation length: 693 residues

MANE

This MANE Select transcript contains ENSP00000408132 and matches to NM_018652.5 and NP_061122.4

Uniprot

This transcript corresponds to the following Uniprot identifiers: A6NDN3

CCDS

This transcript is a member of the Human CCDS set: CCDS10245

Transcript Support Level (TSL)

TSL:1

Version

ENST00000421285.4

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.