Canonical Allele Identifier: CA2339041896
Gene: PRKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.46704304C= , CM000681.2:g.46704304C= GRCh38
NC_000019.9:g.47207561C= , CM000681.1:g.47207561C= GRCh37
NC_000019.8:g.51899401C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000291281.9:c.754G= MANE Select ENSP00000291281.3:p.Glu252=
ENST00000291281.8:c.754G= ENSP00000291281.3:p.Glu252=
ENST00000433867.5:c.754G= ENSP00000393978.1:p.Glu252=
ENST00000595515.5:c.754G= ENSP00000470804.1:p.Glu252=
ENST00000600194.5:c.283G= ENSP00000472744.1:p.Glu95=
ENST00000601605.5:c.41-3192G= ENSP00000470442.1:n.41-3192G=
ENST00000601806.5:c.283G= ENSP00000469106.1:p.Glu95=
NM_001079880.1:c.754G= NP_001073349.1:p.Glu252=
NM_001079881.1:c.754G= NP_001073350.1:p.Glu252=
NM_001079882.1:c.283G= NP_001073351.1:p.Glu95=
NM_016457.4:c.754G= NP_057541.2:p.Glu252=
XM_005258716.2:c.283G= XP_005258773.2:p.Glu95=
NM_001079880.2:c.754G= NP_001073349.1:p.Glu252=
NM_001079881.2:c.754G= NP_001073350.1:p.Glu252=
NM_001079882.2:c.283G= NP_001073351.1:p.Glu95=
NM_016457.5:c.754G= MANE Select NP_057541.2:p.Glu252=