Canonical Allele Identifier: CA3749205

Gene: HLA-DPA1

Linked Data

• dbSNP Id: rs773014134
• ExAC: 6:33036385 A / G
• gnomAD v2: 6-33036385-A-G
• gnomAD v4: 6-33068608-A-G
• MyVariant Identifiers: chr6:g.33036385A>G (hg19) ; chr6:g.33068608A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33068608A>G , CM000668.2:g.33068608A>G	GRCh38
NC_000006.11:g.33036385A>G , CM000668.1:g.33036385A>G	GRCh37
NC_000006.10:g.33144363A>G	NCBI36
NG_033241.1:g.17171T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692443.1:c.*12+30T>C MANE Select	ENSP00000509163.1:n.*12+30T>C
ENST00000419277.5:c.*12+30T>C	ENSP00000393566.1:n.*12+30T>C
ENST00000437811.1:c.427T>C
ENST00000479107.1:n.1424T>C
NM_001242524.1:c.*12+30T>C	NP_001229453.1:n.*12+30T>C
NM_001242525.1:c.*12+30T>C	NP_001229454.1:n.*12+30T>C
NM_033554.3:c.*12+30T>C	NP_291032.2:n.*12+30T>C
XM_011514559.1:c.628+411T>C	XP_011512861.1:n.628+411T>C
NM_001242524.2:c.*12+30T>C	NP_001229453.1:n.*12+30T>C
NM_001242525.2:c.*12+30T>C	NP_001229454.1:n.*12+30T>C