Canonical Allele Identifier: CA3749372

Gene: HLA-DPA1

Linked Data

• dbSNP Id: rs778261553
• ExAC: 6:33037548 G / A
• gnomAD v2: 6-33037548-G-A
• gnomAD v4: 6-33069771-G-A
• MyVariant Identifiers: chr6:g.33037548G>A (hg19) ; chr6:g.33069771G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33069771G>A , CM000668.2:g.33069771G>A	GRCh38
NC_000006.11:g.33037548G>A , CM000668.1:g.33037548G>A	GRCh37
NC_000006.10:g.33145526G>A	NCBI36
NG_033241.1:g.16008C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000692443.1:c.216C>T MANE Select	ENSP00000509163.1:p.Thr72=
ENST00000419277.5:c.216C>T	ENSP00000393566.1:p.Thr72=
ENST00000453337.1:c.216C>T	ENSP00000390929.1:p.Thr72=
ENST00000463066.1:n.311C>T
ENST00000476642.5:n.192C>T
ENST00000479107.1:n.261C>T
NM_001242524.1:c.216C>T	NP_001229453.1:p.Thr72=
NM_001242525.1:c.216C>T	NP_001229454.1:p.Thr72=
NM_033554.3:c.216C>T	NP_291032.2:p.Thr72=
XM_011514559.1:c.216C>T	XP_011512861.1:p.Thr72=
NM_001242524.2:c.216C>T	NP_001229453.1:p.Thr72=
NM_001242525.2:c.216C>T	NP_001229454.1:p.Thr72=