Canonical Allele Identifier: CA1087604171

Gene: HLA-DQA1

Linked Data

• gnomAD v3: 6-32641697-A-T
• gnomAD v4: 6-32641697-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641697A>T , CM000668.2:g.32641697A>T	GRCh38
NC_000006.11:g.32609474A>T , CM000668.1:g.32609474A>T	GRCh37
NC_000006.10:g.32717452A>T	NCBI36
NG_032876.1:g.9292A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.331+139A>T MANE Select	ENSP00000339398.5:n.331+139A>T
ENST00000343139.9:c.331+139A>T	ENSP00000339398.5:n.331+139A>T
ENST00000374949.2:c.331+139A>T	ENSP00000364087.2:n.331+139A>T
ENST00000395363.5:c.331+139A>T	ENSP00000378767.1:n.331+139A>T
ENST00000460633.1:n.359+139A>T
ENST00000482745.5:c.*1163+139A>T	ENSP00000436546.1:n.*1163+139A>T
ENST00000496318.5:c.331+139A>T	ENSP00000437302.1:n.331+139A>T
NM_002122.3:c.331+139A>T	NP_002113.2:n.331+139A>T
XM_006715079.2:c.331+139A>T	XP_006715142.1:n.331+139A>T
XM_006715079.4:c.331+139A>T	XP_006715142.1:n.331+139A>T
XR_001744085.1:n.86+891T>A
NM_002122.5:c.331+139A>T MANE Select	NP_002113.2:n.331+139A>T