Canonical Allele Identifier: CA1087604145
Gene: HLA-DQA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641675_32641676insTT , CM000668.2:g.32641675_32641676insTT GRCh38
NC_000006.11:g.32609452_32609453insTT , CM000668.1:g.32609452_32609453insTT GRCh37
NC_000006.10:g.32717430_32717431insTT NCBI36
NG_032876.1:g.9270_9271insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.331+117_331+118insTT MANE Select ENSP00000339398.5:n.331+117_331+118insTT
ENST00000343139.9:c.331+117_331+118insTT ENSP00000339398.5:n.331+117_331+118insTT
ENST00000374949.2:c.331+117_331+118insTT ENSP00000364087.2:n.331+117_331+118insTT
ENST00000395363.5:c.331+117_331+118insTT ENSP00000378767.1:n.331+117_331+118insTT
ENST00000460633.1:n.359+117_359+118insTT
ENST00000482745.5:c.*1163+117_*1163+118insTT ENSP00000436546.1:n.*1163+117_*1163+118insTT
ENST00000496318.5:c.331+117_331+118insTT ENSP00000437302.1:n.331+117_331+118insTT
NM_002122.3:c.331+117_331+118insTT NP_002113.2:n.331+117_331+118insTT
XM_006715079.2:c.331+117_331+118insTT XP_006715142.1:n.331+117_331+118insTT
XM_006715079.4:c.331+117_331+118insTT XP_006715142.1:n.331+117_331+118insTT
XR_001744085.1:n.86+913_86+914insAA
NM_002122.5:c.331+117_331+118insTT MANE Select NP_002113.2:n.331+117_331+118insTT