Canonical Allele Identifier: CA2770548688
Gene: HLA-DQA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641742_32641766del , CM000668.2:g.32641742_32641766del GRCh38
NC_000006.11:g.32609519_32609543del , CM000668.1:g.32609519_32609543del GRCh37
NC_000006.10:g.32717497_32717521del NCBI36
NG_032876.1:g.9337_9361del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.331+184_332-206del MANE Select ENSP00000339398.5:n.331+184_332-206del
ENST00000343139.9:c.331+184_332-206del ENSP00000339398.5:n.331+184_332-206del
ENST00000374949.2:c.331+184_332-206del ENSP00000364087.2:n.331+184_332-206del
ENST00000395363.5:c.331+184_332-206del ENSP00000378767.1:n.331+184_332-206del
ENST00000460633.1:n.359+184_360-206del
ENST00000482745.5:c.*1163+184_*1164-206del ENSP00000436546.1:n.*1163+184_*1164-206del
ENST00000496318.5:c.331+184_332-206del ENSP00000437302.1:n.331+184_332-206del
NM_002122.3:c.331+184_332-206del NP_002113.2:n.331+184_332-206del
XM_006715079.2:c.331+184_332-206del XP_006715142.1:n.331+184_332-206del
XM_006715079.4:c.331+184_332-206del XP_006715142.1:n.331+184_332-206del
XR_001744085.1:n.86+822_86+846del
NM_002122.5:c.331+184_332-206del MANE Select NP_002113.2:n.331+184_332-206del