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Human (GRCh38.p14)
Description

golgin A8 family member N [Source:HGNC Symbol;Acc:HGNC:44405]

Location

Scaffold HSCHR15_6_CTG8: 2,111,786-2,125,658 forward strand.

GRCh38:KQ031389.1

View this gene on the primary assembly.

About this gene

This gene has 2 transcripts (splice variants) and 1 gene allele.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000635923.2GOLGA8N-2095328632aaENSP00000490331.1
 
Protein coding
A0A1B0GV12 -Ensembl CanonicalGENCODE PrimaryGENCODE Basic
ENST00000643824.1GOLGA8N-2105328632aaENSP00000494486.1
 
Protein coding
A0A1B0GV12 -GENCODE Basic