Canonical Allele Identifier: CA363577308

Gene: HLA-DQA1

Linked Data

• gnomAD v3: 6-32642198-T-G
• gnomAD v4: 6-32642198-T-G
• MyVariant Identifiers: chr6:g.32609975T>G (hg19) ; chr6:g.32642198T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32642198T>G , CM000668.2:g.32642198T>G	GRCh38
NC_000006.11:g.32609975T>G , CM000668.1:g.32609975T>G	GRCh37
NC_000006.10:g.32717953T>G	NCBI36
NG_032876.1:g.9793T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000343139.11:c.558T>G MANE Select	ENSP00000339398.5:p.Ile186Met
ENST00000343139.9:c.558T>G	ENSP00000339398.5:p.Ile186Met
ENST00000374949.2:c.558T>G	ENSP00000364087.2:p.Ile186Met
ENST00000395363.5:c.558T>G	ENSP00000378767.1:p.Ile186Met
ENST00000460633.1:n.586T>G
ENST00000482745.5:c.*1390T>G	ENSP00000436546.1:n.*1390T>G
ENST00000496318.5:c.558T>G	ENSP00000437302.1:p.Ile186Met
NM_002122.3:c.558T>G	NP_002113.2:p.Ile186Met
XM_006715079.2:c.558T>G	XP_006715142.1:p.Ile186Met
XM_006715079.4:c.558T>G	XP_006715142.1:p.Ile186Met
XR_001744085.1:n.86+390A>C
NM_002122.5:c.558T>G MANE Select	NP_002113.2:p.Ile186Met