Canonical Allele Identifier: CA2770548686
Gene: HLA-DQA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641734_32641738del , CM000668.2:g.32641734_32641738del GRCh38
NC_000006.11:g.32609511_32609515del , CM000668.1:g.32609511_32609515del GRCh37
NC_000006.10:g.32717489_32717493del NCBI36
NG_032876.1:g.9329_9333del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.331+176_331+180del MANE Select ENSP00000339398.5:n.331+176_331+180del
ENST00000343139.9:c.331+176_331+180del ENSP00000339398.5:n.331+176_331+180del
ENST00000374949.2:c.331+176_331+180del ENSP00000364087.2:n.331+176_331+180del
ENST00000395363.5:c.331+176_331+180del ENSP00000378767.1:n.331+176_331+180del
ENST00000460633.1:n.359+176_359+180del
ENST00000482745.5:c.*1163+176_*1163+180del ENSP00000436546.1:n.*1163+176_*1163+180del
ENST00000496318.5:c.331+176_331+180del ENSP00000437302.1:n.331+176_331+180del
NM_002122.3:c.331+176_331+180del NP_002113.2:n.331+176_331+180del
XM_006715079.2:c.331+176_331+180del XP_006715142.1:n.331+176_331+180del
XM_006715079.4:c.331+176_331+180del XP_006715142.1:n.331+176_331+180del
XR_001744085.1:n.86+850_86+854del
NM_002122.5:c.331+176_331+180del MANE Select NP_002113.2:n.331+176_331+180del