Canonical Allele Identifier: CA1087604221

Gene: HLA-DQA1

Linked Data

• gnomAD v3: 6-32641747-T-C
• gnomAD v4: 6-32641747-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641747T>C , CM000668.2:g.32641747T>C	GRCh38
NC_000006.11:g.32609524T>C , CM000668.1:g.32609524T>C	GRCh37
NC_000006.10:g.32717502T>C	NCBI36
NG_032876.1:g.9342T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.331+189T>C MANE Select	ENSP00000339398.5:n.331+189T>C
ENST00000343139.9:c.331+189T>C	ENSP00000339398.5:n.331+189T>C
ENST00000374949.2:c.331+189T>C	ENSP00000364087.2:n.331+189T>C
ENST00000395363.5:c.331+189T>C	ENSP00000378767.1:n.331+189T>C
ENST00000460633.1:n.359+189T>C
ENST00000482745.5:c.*1163+189T>C	ENSP00000436546.1:n.*1163+189T>C
ENST00000496318.5:c.331+189T>C	ENSP00000437302.1:n.331+189T>C
NM_002122.3:c.331+189T>C	NP_002113.2:n.331+189T>C
XM_006715079.2:c.331+189T>C	XP_006715142.1:n.331+189T>C
XM_006715079.4:c.331+189T>C	XP_006715142.1:n.331+189T>C
XR_001744085.1:n.86+841A>G
NM_002122.5:c.331+189T>C MANE Select	NP_002113.2:n.331+189T>C