Canonical Allele Identifier: CA3749339

Gene: HLA-DPA1

Linked Data

• dbSNP Id: rs368373459
• ExAC: 6:33037408 T / A
• gnomAD v2: 6-33037408-T-A
• gnomAD v3: 6-33069631-T-A
• gnomAD v4: 6-33069631-T-A
• MyVariant Identifiers: chr6:g.33037408T>A (hg19) ; chr6:g.33069631T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33069631T>A , CM000668.2:g.33069631T>A	GRCh38
NC_000006.11:g.33037408T>A , CM000668.1:g.33037408T>A	GRCh37
NC_000006.10:g.33145386T>A	NCBI36
NG_033241.1:g.16148A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692443.1:c.346+10A>T MANE Select	ENSP00000509163.1:n.346+10A>T
ENST00000419277.5:c.346+10A>T	ENSP00000393566.1:n.346+10A>T
ENST00000453337.1:c.346+10A>T	ENSP00000390929.1:n.346+10A>T
ENST00000463066.1:n.441+10A>T
ENST00000476642.5:n.322+10A>T
ENST00000479107.1:n.401A>T
NM_001242524.1:c.346+10A>T	NP_001229453.1:n.346+10A>T
NM_001242525.1:c.346+10A>T	NP_001229454.1:n.346+10A>T
NM_033554.3:c.346+10A>T	NP_291032.2:n.346+10A>T
XM_011514559.1:c.346+10A>T	XP_011512861.1:n.346+10A>T
NM_001242524.2:c.346+10A>T	NP_001229453.1:n.346+10A>T
NM_001242525.2:c.346+10A>T	NP_001229454.1:n.346+10A>T