Canonical Allele Identifier: CA2559995387
Gene: HLA-DQA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641797_32641798del , CM000668.2:g.32641797_32641798del GRCh38
NC_000006.11:g.32609574_32609575del , CM000668.1:g.32609574_32609575del GRCh37
NC_000006.10:g.32717552_32717553del NCBI36
NG_032876.1:g.9392_9393del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.332-175_332-174del MANE Select ENSP00000339398.5:n.332-175_332-174del
ENST00000343139.9:c.332-175_332-174del ENSP00000339398.5:n.332-175_332-174del
ENST00000374949.2:c.332-175_332-174del ENSP00000364087.2:n.332-175_332-174del
ENST00000395363.5:c.332-175_332-174del ENSP00000378767.1:n.332-175_332-174del
ENST00000460633.1:n.360-175_360-174del
ENST00000482745.5:c.*1164-175_*1164-174del ENSP00000436546.1:n.*1164-175_*1164-174del
ENST00000496318.5:c.332-175_332-174del ENSP00000437302.1:n.332-175_332-174del
NM_002122.3:c.332-175_332-174del NP_002113.2:n.332-175_332-174del
XM_006715079.2:c.332-175_332-174del XP_006715142.1:n.332-175_332-174del
XM_006715079.4:c.332-175_332-174del XP_006715142.1:n.332-175_332-174del
XR_001744085.1:n.86+790_86+791del
NM_002122.5:c.332-175_332-174del MANE Select NP_002113.2:n.332-175_332-174del