Canonical Allele Identifier: CA363608757

Gene: HLA-DPA1

Linked Data

• dbSNP Id: rs1334072731
• gnomAD v2: 6-33037496-C-T
• gnomAD v3: 6-33069719-C-T
• gnomAD v4: 6-33069719-C-T
• MyVariant Identifiers: chr6:g.33037496C>T (hg19) ; chr6:g.33069719C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33069719C>T , CM000668.2:g.33069719C>T	GRCh38
NC_000006.11:g.33037496C>T , CM000668.1:g.33037496C>T	GRCh37
NC_000006.10:g.33145474C>T	NCBI36
NG_033241.1:g.16060G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692443.1:c.268G>A MANE Select	ENSP00000509163.1:p.Gly90Arg
ENST00000419277.5:c.268G>A	ENSP00000393566.1:p.Gly90Arg
ENST00000453337.1:c.268G>A	ENSP00000390929.1:p.Gly90Arg
ENST00000463066.1:n.363G>A
ENST00000476642.5:n.244G>A
ENST00000479107.1:n.313G>A
NM_001242524.1:c.268G>A	NP_001229453.1:p.Gly90Arg
NM_001242525.1:c.268G>A	NP_001229454.1:p.Gly90Arg
NM_033554.3:c.268G>A	NP_291032.2:p.Gly90Arg
XM_011514559.1:c.268G>A	XP_011512861.1:p.Gly90Arg
NM_001242524.2:c.268G>A	NP_001229453.1:p.Gly90Arg
NM_001242525.2:c.268G>A	NP_001229454.1:p.Gly90Arg