Canonical Allele Identifier: CA1087604143
Gene: HLA-DQA1 HGNC NCBI

Linked Data

gnomAD v3: 6-32641673-C-A
gnomAD v4: 6-32641673-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641673C>A , CM000668.2:g.32641673C>A GRCh38
NC_000006.11:g.32609450C>A , CM000668.1:g.32609450C>A GRCh37
NC_000006.10:g.32717428C>A NCBI36
NG_032876.1:g.9268C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.331+115C>A MANE Select ENSP00000339398.5:n.331+115C>A
ENST00000343139.9:c.331+115C>A ENSP00000339398.5:n.331+115C>A
ENST00000374949.2:c.331+115C>A ENSP00000364087.2:n.331+115C>A
ENST00000395363.5:c.331+115C>A ENSP00000378767.1:n.331+115C>A
ENST00000460633.1:n.359+115C>A
ENST00000482745.5:c.*1163+115C>A ENSP00000436546.1:n.*1163+115C>A
ENST00000496318.5:c.331+115C>A ENSP00000437302.1:n.331+115C>A
NM_002122.3:c.331+115C>A NP_002113.2:n.331+115C>A
XM_006715079.2:c.331+115C>A XP_006715142.1:n.331+115C>A
XM_006715079.4:c.331+115C>A XP_006715142.1:n.331+115C>A
XR_001744085.1:n.86+915G>T
NM_002122.5:c.331+115C>A MANE Select NP_002113.2:n.331+115C>A
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