Canonical Allele Identifier: CA1619666882
Gene: HLA-DQA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641803A= , CM000668.2:g.32641803A= GRCh38
NC_000006.11:g.32609580A= , CM000668.1:g.32609580A= GRCh37
NC_000006.10:g.32717558A= NCBI36
NG_032876.1:g.9398A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.332-169A= MANE Select ENSP00000339398.5:n.332-169A=
ENST00000343139.9:c.332-169A= ENSP00000339398.5:n.332-169A=
ENST00000374949.2:c.332-169A= ENSP00000364087.2:n.332-169A=
ENST00000395363.5:c.332-169A= ENSP00000378767.1:n.332-169A=
ENST00000460633.1:n.360-169A=
ENST00000482745.5:c.*1164-169A= ENSP00000436546.1:n.*1164-169A=
ENST00000496318.5:c.332-169A= ENSP00000437302.1:n.332-169A=
NM_002122.3:c.332-169A= NP_002113.2:n.332-169A=
XM_006715079.2:c.332-169A= XP_006715142.1:n.332-169A=
XM_006715079.4:c.332-169A= XP_006715142.1:n.332-169A=
XR_001744085.1:n.86+785T=
NM_002122.5:c.332-169A= MANE Select NP_002113.2:n.332-169A=