Canonical Allele Identifier: CA2339042394

Gene: PRKD2

Linked Data

• dbSNP Id: rs1427649246

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46705285C>G , CM000681.2:g.46705285C>G	GRCh38
NC_000019.9:g.47208542C>G , CM000681.1:g.47208542C>G	GRCh37
NC_000019.8:g.51900382C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000291281.9:c.512-636G>C MANE Select	ENSP00000291281.3:n.512-636G>C
ENST00000291281.8:c.512-636G>C	ENSP00000291281.3:n.512-636G>C
ENST00000433867.5:c.512-636G>C	ENSP00000393978.1:n.512-636G>C
ENST00000595132.5:c.41-636G>C	ENSP00000470363.1:n.41-636G>C
ENST00000595515.5:c.512-636G>C	ENSP00000470804.1:n.512-636G>C
ENST00000597641.1:c.247-636G>C	ENSP00000469064.1:n.247-636G>C
ENST00000598633.1:c.41-636G>C	ENSP00000470919.1:n.41-636G>C
ENST00000600194.5:c.41-636G>C	ENSP00000472744.1:n.41-636G>C
ENST00000601605.5:c.41-4173G>C	ENSP00000470442.1:n.41-4173G>C
ENST00000601806.5:c.41-636G>C	ENSP00000469106.1:n.41-636G>C
NM_001079880.1:c.512-636G>C	NP_001073349.1:n.512-636G>C
NM_001079881.1:c.512-636G>C	NP_001073350.1:n.512-636G>C
NM_001079882.1:c.41-636G>C	NP_001073351.1:n.41-636G>C
NM_016457.4:c.512-636G>C	NP_057541.2:n.512-636G>C
XM_005258716.2:c.41-636G>C	XP_005258773.2:n.41-636G>C
NM_001079880.2:c.512-636G>C	NP_001073349.1:n.512-636G>C
NM_001079881.2:c.512-636G>C	NP_001073350.1:n.512-636G>C
NM_001079882.2:c.41-636G>C	NP_001073351.1:n.41-636G>C
NM_016457.5:c.512-636G>C MANE Select	NP_057541.2:n.512-636G>C