Canonical Allele Identifier: CA363577304

Gene: HLA-DQA1

Linked Data

• gnomAD v3: 6-32642196-A-T
• gnomAD v4: 6-32642196-A-T
• MyVariant Identifiers: chr6:g.32609973A>T (hg19) ; chr6:g.32642196A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32642196A>T , CM000668.2:g.32642196A>T	GRCh38
NC_000006.11:g.32609973A>T , CM000668.1:g.32609973A>T	GRCh37
NC_000006.10:g.32717951A>T	NCBI36
NG_032876.1:g.9791A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000343139.11:c.556A>T MANE Select	ENSP00000339398.5:p.Ile186Phe
ENST00000343139.9:c.556A>T	ENSP00000339398.5:p.Ile186Phe
ENST00000374949.2:c.556A>T	ENSP00000364087.2:p.Ile186Phe
ENST00000395363.5:c.556A>T	ENSP00000378767.1:p.Ile186Phe
ENST00000460633.1:n.584A>T
ENST00000482745.5:c.*1388A>T	ENSP00000436546.1:n.*1388A>T
ENST00000496318.5:c.556A>T	ENSP00000437302.1:p.Ile186Phe
NM_002122.3:c.556A>T	NP_002113.2:p.Ile186Phe
XM_006715079.2:c.556A>T	XP_006715142.1:p.Ile186Phe
XM_006715079.4:c.556A>T	XP_006715142.1:p.Ile186Phe
XR_001744085.1:n.86+392T>A
NM_002122.5:c.556A>T MANE Select	NP_002113.2:p.Ile186Phe