Canonical Allele Identifier: CA3749395

Gene: HLA-DPA1

Linked Data

• dbSNP Id: rs571030506
• ExAC: 6:33037641 G / A
• gnomAD v2: 6-33037641-G-A
• gnomAD v3: 6-33069864-G-A
• gnomAD v4: 6-33069864-G-A
• MyVariant Identifiers: chr6:g.33037641G>A (hg19) ; chr6:g.33069864G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33069864G>A , CM000668.2:g.33069864G>A	GRCh38
NC_000006.11:g.33037641G>A , CM000668.1:g.33037641G>A	GRCh37
NC_000006.10:g.33145619G>A	NCBI36
NG_033241.1:g.15915C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692443.1:c.123C>T MANE Select	ENSP00000509163.1:p.Ala41=
ENST00000419277.5:c.123C>T	ENSP00000393566.1:p.Ala41=
ENST00000453337.1:c.123C>T	ENSP00000390929.1:p.Ala41=
ENST00000463066.1:n.218C>T
ENST00000476642.5:n.99C>T
ENST00000479107.1:n.168C>T
NM_001242524.1:c.123C>T	NP_001229453.1:p.Ala41=
NM_001242525.1:c.123C>T	NP_001229454.1:p.Ala41=
NM_033554.3:c.123C>T	NP_291032.2:p.Ala41=
XM_011514559.1:c.123C>T	XP_011512861.1:p.Ala41=
NM_001242524.2:c.123C>T	NP_001229453.1:p.Ala41=
NM_001242525.2:c.123C>T	NP_001229454.1:p.Ala41=