Canonical Allele Identifier: CA363577108

Gene: HLA-DQA1

Linked Data

• gnomAD v3: 6-32642104-C-G
• gnomAD v4: 6-32642104-C-G
• MyVariant Identifiers: chr6:g.32609881C>G (hg19) ; chr6:g.32642104C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32642104C>G , CM000668.2:g.32642104C>G	GRCh38
NC_000006.11:g.32609881C>G , CM000668.1:g.32609881C>G	GRCh37
NC_000006.10:g.32717859C>G	NCBI36
NG_032876.1:g.9699C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.464C>G MANE Select	ENSP00000339398.5:p.Thr155Arg
ENST00000343139.9:c.464C>G	ENSP00000339398.5:p.Thr155Arg
ENST00000374949.2:c.464C>G	ENSP00000364087.2:p.Thr155Arg
ENST00000395363.5:c.464C>G	ENSP00000378767.1:p.Thr155Arg
ENST00000460633.1:n.492C>G
ENST00000482745.5:c.*1296C>G	ENSP00000436546.1:n.*1296C>G
ENST00000496318.5:c.464C>G	ENSP00000437302.1:p.Thr155Arg
NM_002122.3:c.464C>G	NP_002113.2:p.Thr155Arg
XM_006715079.2:c.464C>G	XP_006715142.1:p.Thr155Arg
XM_006715079.4:c.464C>G	XP_006715142.1:p.Thr155Arg
XR_001744085.1:n.86+484G>C
NM_002122.5:c.464C>G MANE Select	NP_002113.2:p.Thr155Arg