Canonical Allele Identifier: CA363577307

Gene: HLA-DQA1

Linked Data

• gnomAD v3: 6-32642197-T-C
• gnomAD v4: 6-32642197-T-C
• MyVariant Identifiers: chr6:g.32609974T>C (hg19) ; chr6:g.32642197T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32642197T>C , CM000668.2:g.32642197T>C	GRCh38
NC_000006.11:g.32609974T>C , CM000668.1:g.32609974T>C	GRCh37
NC_000006.10:g.32717952T>C	NCBI36
NG_032876.1:g.9792T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000343139.11:c.557T>C MANE Select	ENSP00000339398.5:p.Ile186Thr
ENST00000343139.9:c.557T>C	ENSP00000339398.5:p.Ile186Thr
ENST00000374949.2:c.557T>C	ENSP00000364087.2:p.Ile186Thr
ENST00000395363.5:c.557T>C	ENSP00000378767.1:p.Ile186Thr
ENST00000460633.1:n.585T>C
ENST00000482745.5:c.*1389T>C	ENSP00000436546.1:n.*1389T>C
ENST00000496318.5:c.557T>C	ENSP00000437302.1:p.Ile186Thr
NM_002122.3:c.557T>C	NP_002113.2:p.Ile186Thr
XM_006715079.2:c.557T>C	XP_006715142.1:p.Ile186Thr
XM_006715079.4:c.557T>C	XP_006715142.1:p.Ile186Thr
XR_001744085.1:n.86+391A>G
NM_002122.5:c.557T>C MANE Select	NP_002113.2:p.Ile186Thr