Canonical Allele Identifier: CA1087604292
Gene: HLA-DQA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641841_32641845del , CM000668.2:g.32641841_32641845del GRCh38
NC_000006.11:g.32609618_32609622del , CM000668.1:g.32609618_32609622del GRCh37
NC_000006.10:g.32717596_32717600del NCBI36
NG_032876.1:g.9436_9440del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.332-131_332-127del MANE Select ENSP00000339398.5:n.332-131_332-127del
ENST00000343139.9:c.332-131_332-127del ENSP00000339398.5:n.332-131_332-127del
ENST00000374949.2:c.332-131_332-127del ENSP00000364087.2:n.332-131_332-127del
ENST00000395363.5:c.332-131_332-127del ENSP00000378767.1:n.332-131_332-127del
ENST00000460633.1:n.360-131_360-127del
ENST00000482745.5:c.*1164-131_*1164-127del ENSP00000436546.1:n.*1164-131_*1164-127del
ENST00000496318.5:c.332-131_332-127del ENSP00000437302.1:n.332-131_332-127del
NM_002122.3:c.332-131_332-127del NP_002113.2:n.332-131_332-127del
XM_006715079.2:c.332-131_332-127del XP_006715142.1:n.332-131_332-127del
XM_006715079.4:c.332-131_332-127del XP_006715142.1:n.332-131_332-127del
XR_001744085.1:n.86+744_86+748del
NM_002122.5:c.332-131_332-127del MANE Select NP_002113.2:n.332-131_332-127del