Canonical Allele Identifier: CA406488978

Gene: PRKD2

Linked Data

• dbSNP Id: rs2053677746
• COSMIC: COSM712228
• MyVariant Identifiers: chr19:g.47207510T>C (hg19) ; chr19:g.46704253T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46704253T>C , CM000681.2:g.46704253T>C	GRCh38
NC_000019.9:g.47207510T>C , CM000681.1:g.47207510T>C	GRCh37
NC_000019.8:g.51899350T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291281.9:c.805A>G MANE Select	ENSP00000291281.3:p.Ile269Val
ENST00000291281.8:c.805A>G	ENSP00000291281.3:p.Ile269Val
ENST00000433867.5:c.805A>G	ENSP00000393978.1:p.Ile269Val
ENST00000595515.5:c.805A>G	ENSP00000470804.1:p.Ile269Val
ENST00000600194.5:c.334A>G	ENSP00000472744.1:p.Ile112Val
ENST00000601605.5:c.41-3141A>G	ENSP00000470442.1:n.41-3141A>G
ENST00000601806.5:c.334A>G	ENSP00000469106.1:p.Ile112Val
NM_001079880.1:c.805A>G	NP_001073349.1:p.Ile269Val
NM_001079881.1:c.805A>G	NP_001073350.1:p.Ile269Val
NM_001079882.1:c.334A>G	NP_001073351.1:p.Ile112Val
NM_016457.4:c.805A>G	NP_057541.2:p.Ile269Val
XM_005258716.2:c.334A>G	XP_005258773.2:p.Ile112Val
NM_001079880.2:c.805A>G	NP_001073349.1:p.Ile269Val
NM_001079881.2:c.805A>G	NP_001073350.1:p.Ile269Val
NM_001079882.2:c.334A>G	NP_001073351.1:p.Ile112Val
NM_016457.5:c.805A>G MANE Select	NP_057541.2:p.Ile269Val