Human (GRCh38.p14)
Description

golgin A8 family member O [Source:HGNC Symbol;Acc:HGNC:44406]

Location
About this transcript

This transcript has 19 exons, is annotated with 23 domains and features, is associated with 4361 variant alleles and maps to 3839 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000509311.7GOLGA8O-2015189632aaENSP00000423159.2
 
Protein coding
CCDS59252A6NCC3-2 NM_001277308.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000562377.1GOLGA8O-202555131aaENSP00000456713.1
 
Protein coding
H3BSI0 -TSL:4CDS 3' incomplete
Statistics

Exons: 19, Coding exons: 19, Transcript length: 5,189 bps, Translation length: 632 residues

MANE

This MANE Select transcript contains ENSP00000423159 and matches to NM_001277308.1 and NP_001264237.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: A6NCC3

CCDS

This transcript is a member of the Human CCDS set: CCDS59252

Transcript Support Level (TSL)

TSL:5

Version

ENST00000509311.7

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.

Annotation Attributes

dotter confirmed [Definitions]

GENCODE basic gene

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