Canonical Allele Identifier: CA882830256

Gene: PRKD2

Linked Data

• dbSNP Id: rs1390628810
• MyVariant Identifiers: chr19:g.47207359A>G (hg19) ; chr19:g.46704102A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46704102A>G , CM000681.2:g.46704102A>G	GRCh38
NC_000019.9:g.47207359A>G , CM000681.1:g.47207359A>G	GRCh37
NC_000019.8:g.51899199A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291281.9:c.889+67T>C MANE Select	ENSP00000291281.3:n.889+67T>C
ENST00000291281.8:c.889+67T>C	ENSP00000291281.3:n.889+67T>C
ENST00000433867.5:c.889+67T>C	ENSP00000393978.1:n.889+67T>C
ENST00000595515.5:c.889+67T>C	ENSP00000470804.1:n.889+67T>C
ENST00000600194.5:c.418+67T>C	ENSP00000472744.1:n.418+67T>C
ENST00000601605.5:c.41-2990T>C	ENSP00000470442.1:n.41-2990T>C
ENST00000601806.5:c.418+67T>C	ENSP00000469106.1:n.418+67T>C
NM_001079880.1:c.889+67T>C	NP_001073349.1:n.889+67T>C
NM_001079881.1:c.889+67T>C	NP_001073350.1:n.889+67T>C
NM_001079882.1:c.418+67T>C	NP_001073351.1:n.418+67T>C
NM_016457.4:c.889+67T>C	NP_057541.2:n.889+67T>C
XM_005258716.2:c.418+67T>C	XP_005258773.2:n.418+67T>C
NM_001079880.2:c.889+67T>C	NP_001073349.1:n.889+67T>C
NM_001079881.2:c.889+67T>C	NP_001073350.1:n.889+67T>C
NM_001079882.2:c.418+67T>C	NP_001073351.1:n.418+67T>C
NM_016457.5:c.889+67T>C MANE Select	NP_057541.2:n.889+67T>C