Canonical Allele Identifier: CA1087604313
Gene: HLA-DQA1 HGNC NCBI

Linked Data

gnomAD v3: 6-32641853-T-G
gnomAD v4: 6-32641853-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641853T>G , CM000668.2:g.32641853T>G GRCh38
NC_000006.11:g.32609630T>G , CM000668.1:g.32609630T>G GRCh37
NC_000006.10:g.32717608T>G NCBI36
NG_032876.1:g.9448T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.332-119T>G MANE Select ENSP00000339398.5:n.332-119T>G
ENST00000343139.9:c.332-119T>G ENSP00000339398.5:n.332-119T>G
ENST00000374949.2:c.332-119T>G ENSP00000364087.2:n.332-119T>G
ENST00000395363.5:c.332-119T>G ENSP00000378767.1:n.332-119T>G
ENST00000460633.1:n.360-119T>G
ENST00000482745.5:c.*1164-119T>G ENSP00000436546.1:n.*1164-119T>G
ENST00000496318.5:c.332-119T>G ENSP00000437302.1:n.332-119T>G
NM_002122.3:c.332-119T>G NP_002113.2:n.332-119T>G
XM_006715079.2:c.332-119T>G XP_006715142.1:n.332-119T>G
XM_006715079.4:c.332-119T>G XP_006715142.1:n.332-119T>G
XR_001744085.1:n.86+735A>C
NM_002122.5:c.332-119T>G MANE Select NP_002113.2:n.332-119T>G
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