Canonical Allele Identifier: CA363577293

Gene: HLA-DQA1

Linked Data

• gnomAD v3: 6-32642191-A-T
• gnomAD v4: 6-32642191-A-T
• MyVariant Identifiers: chr6:g.32609968A>T (hg19) ; chr6:g.32642191A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32642191A>T , CM000668.2:g.32642191A>T	GRCh38
NC_000006.11:g.32609968A>T , CM000668.1:g.32609968A>T	GRCh37
NC_000006.10:g.32717946A>T	NCBI36
NG_032876.1:g.9786A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000343139.11:c.551A>T MANE Select	ENSP00000339398.5:p.Asp184Val
ENST00000343139.9:c.551A>T	ENSP00000339398.5:p.Asp184Val
ENST00000374949.2:c.551A>T	ENSP00000364087.2:p.Asp184Val
ENST00000395363.5:c.551A>T	ENSP00000378767.1:p.Asp184Val
ENST00000460633.1:n.579A>T
ENST00000482745.5:c.*1383A>T	ENSP00000436546.1:n.*1383A>T
ENST00000496318.5:c.551A>T	ENSP00000437302.1:p.Asp184Val
NM_002122.3:c.551A>T	NP_002113.2:p.Asp184Val
XM_006715079.2:c.551A>T	XP_006715142.1:p.Asp184Val
XM_006715079.4:c.551A>T	XP_006715142.1:p.Asp184Val
XR_001744085.1:n.86+397T>A
NM_002122.5:c.551A>T MANE Select	NP_002113.2:p.Asp184Val