Canonical Allele Identifier: CA2678168104
Gene: HLA-DQA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641674_32641675insGT , CM000668.2:g.32641674_32641675insGT GRCh38
NC_000006.11:g.32609451_32609452insGT , CM000668.1:g.32609451_32609452insGT GRCh37
NC_000006.10:g.32717429_32717430insGT NCBI36
NG_032876.1:g.9269_9270insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.331+116_331+117insGT MANE Select ENSP00000339398.5:n.331+116_331+117insGT
ENST00000343139.9:c.331+116_331+117insGT ENSP00000339398.5:n.331+116_331+117insGT
ENST00000374949.2:c.331+116_331+117insGT ENSP00000364087.2:n.331+116_331+117insGT
ENST00000395363.5:c.331+116_331+117insGT ENSP00000378767.1:n.331+116_331+117insGT
ENST00000460633.1:n.359+116_359+117insGT
ENST00000482745.5:c.*1163+116_*1163+117insGT ENSP00000436546.1:n.*1163+116_*1163+117insGT
ENST00000496318.5:c.331+116_331+117insGT ENSP00000437302.1:n.331+116_331+117insGT
NM_002122.3:c.331+116_331+117insGT NP_002113.2:n.331+116_331+117insGT
XM_006715079.2:c.331+116_331+117insGT XP_006715142.1:n.331+116_331+117insGT
XM_006715079.4:c.331+116_331+117insGT XP_006715142.1:n.331+116_331+117insGT
XR_001744085.1:n.86+913_86+914insAC
NM_002122.5:c.331+116_331+117insGT MANE Select NP_002113.2:n.331+116_331+117insGT