Canonical Allele Identifier: CA363577290

Gene: HLA-DQA1

Linked Data

• gnomAD v4: 6-32642190-G-T
• MyVariant Identifiers: chr6:g.32609967G>T (hg19) ; chr6:g.32642190G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32642190G>T , CM000668.2:g.32642190G>T	GRCh38
NC_000006.11:g.32609967G>T , CM000668.1:g.32609967G>T	GRCh37
NC_000006.10:g.32717945G>T	NCBI36
NG_032876.1:g.9785G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000343139.11:c.550G>T MANE Select	ENSP00000339398.5:p.Asp184Tyr
ENST00000343139.9:c.550G>T	ENSP00000339398.5:p.Asp184Tyr
ENST00000374949.2:c.550G>T	ENSP00000364087.2:p.Asp184Tyr
ENST00000395363.5:c.550G>T	ENSP00000378767.1:p.Asp184Tyr
ENST00000460633.1:n.578G>T
ENST00000482745.5:c.*1382G>T	ENSP00000436546.1:n.*1382G>T
ENST00000496318.5:c.550G>T	ENSP00000437302.1:p.Asp184Tyr
NM_002122.3:c.550G>T	NP_002113.2:p.Asp184Tyr
XM_006715079.2:c.550G>T	XP_006715142.1:p.Asp184Tyr
XM_006715079.4:c.550G>T	XP_006715142.1:p.Asp184Tyr
XR_001744085.1:n.86+398C>A
NM_002122.5:c.550G>T MANE Select	NP_002113.2:p.Asp184Tyr