Canonical Allele Identifier: CA1619667002
Gene: HLA-DQA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32642079T= , CM000668.2:g.32642079T= GRCh38
NC_000006.11:g.32609856T= , CM000668.1:g.32609856T= GRCh37
NC_000006.10:g.32717834T= NCBI36
NG_032876.1:g.9674T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.439T= MANE Select ENSP00000339398.5:p.Trp147=
ENST00000343139.9:c.439T= ENSP00000339398.5:p.Trp147=
ENST00000374949.2:c.439T= ENSP00000364087.2:p.Trp147=
ENST00000395363.5:c.439T= ENSP00000378767.1:p.Trp147=
ENST00000460633.1:n.467T=
ENST00000482745.5:c.*1271T= ENSP00000436546.1:n.*1271T=
ENST00000496318.5:c.439T= ENSP00000437302.1:p.Trp147=
NM_002122.3:c.439T= NP_002113.2:p.Trp147=
XM_006715079.2:c.439T= XP_006715142.1:p.Trp147=
XM_006715079.4:c.439T= XP_006715142.1:p.Trp147=
XR_001744085.1:n.86+509A=
NM_002122.5:c.439T= MANE Select NP_002113.2:p.Trp147=