Human (GRCh38.p14)
Description

golgin A6 family like 22 [Source:HGNC Symbol;Acc:HGNC:50289]

Location
About this transcript

This transcript has 9 exons, is annotated with 22 domains and features, is associated with 4954 variant alleles and maps to 1725 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000622895.2GOLGA6L22-2034401854aaENSP00000483673.2
 
Protein coding
CCDS91962H0YM25 NM_001396956.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
Statistics

Exons: 9, Coding exons: 8, Transcript length: 4,401 bps, Translation length: 854 residues

MANE

This MANE Select transcript contains ENSP00000483673 and matches to NM_001396956.1 and NP_001383885.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: H0YM25

CCDS

This transcript is a member of the Human CCDS set: CCDS91962

Transcript Support Level (TSL)

TSL:5

Version

ENST00000622895.2

Type

Protein coding

Annotation Method

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

Annotation Attributes

inferred exon combination [Definitions]

GENCODE basic gene

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