Canonical Allele Identifier: CA507974878

Gene: PRKD2

Linked Data

• MyVariant Identifiers: chr19:g.47207568G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46704311G>A , CM000681.2:g.46704311G>A	GRCh38
NC_000019.9:g.47207568G>A , CM000681.1:g.47207568G>A	GRCh37
NC_000019.8:g.51899408G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000291281.9:c.747C>T MANE Select	ENSP00000291281.3:p.Arg249=
ENST00000291281.8:c.747C>T	ENSP00000291281.3:p.Arg249=
ENST00000433867.5:c.747C>T	ENSP00000393978.1:p.Arg249=
ENST00000595515.5:c.747C>T	ENSP00000470804.1:p.Arg249=
ENST00000600194.5:c.276C>T	ENSP00000472744.1:p.Arg92=
ENST00000601605.5:c.41-3199C>T	ENSP00000470442.1:n.41-3199C>T
ENST00000601806.5:c.276C>T	ENSP00000469106.1:p.Arg92=
NM_001079880.1:c.747C>T	NP_001073349.1:p.Arg249=
NM_001079881.1:c.747C>T	NP_001073350.1:p.Arg249=
NM_001079882.1:c.276C>T	NP_001073351.1:p.Arg92=
NM_016457.4:c.747C>T	NP_057541.2:p.Arg249=
XM_005258716.2:c.276C>T	XP_005258773.2:p.Arg92=
NM_001079880.2:c.747C>T	NP_001073349.1:p.Arg249=
NM_001079881.2:c.747C>T	NP_001073350.1:p.Arg249=
NM_001079882.2:c.276C>T	NP_001073351.1:p.Arg92=
NM_016457.5:c.747C>T MANE Select	NP_057541.2:p.Arg249=