Canonical Allele Identifier: CA1619666861
Gene: HLA-DQA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641748A= , CM000668.2:g.32641748A= GRCh38
NC_000006.11:g.32609525A= , CM000668.1:g.32609525A= GRCh37
NC_000006.10:g.32717503A= NCBI36
NG_032876.1:g.9343A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.331+190A= MANE Select ENSP00000339398.5:n.331+190A=
ENST00000343139.9:c.331+190A= ENSP00000339398.5:n.331+190A=
ENST00000374949.2:c.331+190A= ENSP00000364087.2:n.331+190A=
ENST00000395363.5:c.331+190A= ENSP00000378767.1:n.331+190A=
ENST00000460633.1:n.359+190A=
ENST00000482745.5:c.*1163+190A= ENSP00000436546.1:n.*1163+190A=
ENST00000496318.5:c.331+190A= ENSP00000437302.1:n.331+190A=
NM_002122.3:c.331+190A= NP_002113.2:n.331+190A=
XM_006715079.2:c.331+190A= XP_006715142.1:n.331+190A=
XM_006715079.4:c.331+190A= XP_006715142.1:n.331+190A=
XR_001744085.1:n.86+840T=
NM_002122.5:c.331+190A= MANE Select NP_002113.2:n.331+190A=
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