Human (GRCh38.p14)
Description

golgin A6 family like 2 [Source:HGNC Symbol;Acc:HGNC:26695]

Gene Synonyms

CT105, FLJ36144

Location
About this transcript

This transcript has 8 exons, is annotated with 31 domains and features, is associated with 5987 variant alleles and maps to 581 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000567107.6GOLGA6L2-2023499909aaENSP00000454407.1
 
Protein coding
CCDS76728Q8N9W4-3 NM_001304388.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000566571.5GOLGA6L2-2012938208aaENSP00000456523.1
 
Nonsense mediated decay
H3BS38 -TSL:5
Statistics

Exons: 8, Coding exons: 8, Transcript length: 3,499 bps, Translation length: 909 residues

MANE

This MANE Select transcript contains ENSP00000454407 and matches to NM_001304388.2 and NP_001291317.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8N9W4

CCDS

This transcript is a member of the Human CCDS set: CCDS76728

Transcript Support Level (TSL)

TSL:5

Version

ENST00000567107.6

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.