Canonical Allele Identifier: CA406489048

Gene: PRKD2

Linked Data

• MyVariant Identifiers: chr19:g.47207533A>T (hg19) ; chr19:g.46704276A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46704276A>T , CM000681.2:g.46704276A>T	GRCh38
NC_000019.9:g.47207533A>T , CM000681.1:g.47207533A>T	GRCh37
NC_000019.8:g.51899373A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291281.9:c.782T>A MANE Select	ENSP00000291281.3:p.Val261Asp
ENST00000291281.8:c.782T>A	ENSP00000291281.3:p.Val261Asp
ENST00000433867.5:c.782T>A	ENSP00000393978.1:p.Val261Asp
ENST00000595515.5:c.782T>A	ENSP00000470804.1:p.Val261Asp
ENST00000600194.5:c.311T>A	ENSP00000472744.1:p.Val104Asp
ENST00000601605.5:c.41-3164T>A	ENSP00000470442.1:n.41-3164T>A
ENST00000601806.5:c.311T>A	ENSP00000469106.1:p.Val104Asp
NM_001079880.1:c.782T>A	NP_001073349.1:p.Val261Asp
NM_001079881.1:c.782T>A	NP_001073350.1:p.Val261Asp
NM_001079882.1:c.311T>A	NP_001073351.1:p.Val104Asp
NM_016457.4:c.782T>A	NP_057541.2:p.Val261Asp
XM_005258716.2:c.311T>A	XP_005258773.2:p.Val104Asp
NM_001079880.2:c.782T>A	NP_001073349.1:p.Val261Asp
NM_001079881.2:c.782T>A	NP_001073350.1:p.Val261Asp
NM_001079882.2:c.311T>A	NP_001073351.1:p.Val104Asp
NM_016457.5:c.782T>A MANE Select	NP_057541.2:p.Val261Asp