Human (GRCh38.p14)
Description

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

Location

Chromosome 15: 32,593,456-32,607,310 forward strand.

GRCh38:CM000677.2

View alleles of this gene on alternative sequences

About this gene

This gene has 8 transcripts (splice variants), 1 gene allele, 248 orthologues and 18 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000448387.7GOLGA8N-2015256632aaENSP00000398454.2
 
Protein coding
CCDS61578F8WBI6 NM_001282494.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000569659.6GOLGA8N-2055221596aaENSP00000454473.1
 
Protein coding
H3BMP0 -GENCODE basicTSL:5
ENST00000611209.1GOLGA8N-207555No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000605665.1GOLGA8N-206271No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000453952.3GOLGA8N-2021385No protein-
 
Retained intron
--TSL:NA
ENST00000695847.1GOLGA8N-2081356No protein-
 
Retained intron
---
ENST00000569536.1GOLGA8N-2041212No protein-
 
Retained intron
--TSL:1
ENST00000567075.1GOLGA8N-203584No protein-
 
Retained intron
--TSL:4