Canonical Allele Identifier: CA824032609

Gene: HLA-DPA1

Linked Data

• dbSNP Id: rs1293563541
• MyVariant Identifiers: chr6:g.33037357A>G (hg19) ; chr6:g.33069580A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33069580A>G , CM000668.2:g.33069580A>G	GRCh38
NC_000006.11:g.33037357A>G , CM000668.1:g.33037357A>G	GRCh37
NC_000006.10:g.33145335A>G	NCBI36
NG_033241.1:g.16199T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692443.1:c.346+61T>C MANE Select	ENSP00000509163.1:n.346+61T>C
ENST00000419277.5:c.346+61T>C	ENSP00000393566.1:n.346+61T>C
ENST00000453337.1:c.346+61T>C	ENSP00000390929.1:n.346+61T>C
ENST00000463066.1:n.441+61T>C
ENST00000476642.5:n.322+61T>C
ENST00000479107.1:n.452T>C
NM_001242524.1:c.346+61T>C	NP_001229453.1:n.346+61T>C
NM_001242525.1:c.346+61T>C	NP_001229454.1:n.346+61T>C
NM_033554.3:c.346+61T>C	NP_291032.2:n.346+61T>C
XM_011514559.1:c.346+61T>C	XP_011512861.1:n.346+61T>C
NM_001242524.2:c.346+61T>C	NP_001229453.1:n.346+61T>C
NM_001242525.2:c.346+61T>C	NP_001229454.1:n.346+61T>C