Canonical Allele Identifier: CA3743738
Gene: HLA-DQA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1258533
ClinVar RCV Id: RCV001671063
dbSNP Id: rs1129740
gnomAD v2: 6-32609105-G-A
gnomAD v3: 6-32641328-G-A
gnomAD v4: 6-32641328-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641328G>A , CM000668.2:g.32641328G>A GRCh38
NC_000006.11:g.32609105G>A , CM000668.1:g.32609105G>A GRCh37
NC_000006.10:g.32717083G>A NCBI36
NG_032876.1:g.8923G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343139.11:c.101G>A MANE Select ENSP00000339398.5:p.Cys34Tyr
ENST00000343139.9:c.101G>A ENSP00000339398.5:p.Cys34Tyr
ENST00000374949.2:c.101G>A ENSP00000364087.2:p.Cys34Tyr
ENST00000395363.5:c.101G>A ENSP00000378767.1:p.Cys34Tyr
ENST00000460633.1:n.129G>A
ENST00000482745.5:c.*933G>A ENSP00000436546.1:n.*933G>A
ENST00000496318.5:c.101G>A ENSP00000437302.1:p.Cys34Tyr
NM_002122.3:c.101G>A NP_002113.2:p.Cys34Tyr
XM_006715079.2:c.101G>A XP_006715142.1:p.Cys34Tyr
XM_006715079.4:c.101G>A XP_006715142.1:p.Cys34Tyr
XR_001744085.1:n.87-847C>T
NM_002122.5:c.101G>A MANE Select NP_002113.2:p.Cys34Tyr