Canonical Allele Identifier: CA344633

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 42166
• ClinVar RCV Id: RCV000034993
• dbSNP Id: rs386134166
• MyVariant Identifiers: chr19:g.54392997T>C (hg19) ; chr19:g.53889743T>C (hg38)
• PubMed: PMID:16649092 ; PMID:20301573

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889743T>C , CM000681.2:g.53889743T>C	GRCh38
NC_000019.9:g.54392997T>C , CM000681.1:g.54392997T>C	GRCh37
NC_000019.8:g.59084809T>C	NCBI36
NG_009114.1:g.12531T>C , LRG_669:g.12531T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.391T>C	ENSP00000507230.1:p.Cys131Arg
ENST00000682268.1:n.689T>C
ENST00000682902.1:n.693T>C
ENST00000683513.1:c.391T>C	ENSP00000506809.1:p.Cys131Arg
ENST00000263431.4:c.391T>C MANE Select	ENSP00000263431.3:p.Cys131Arg
ENST00000263431.3:c.391T>C	ENSP00000263431.3:p.Cys131Arg
ENST00000419486.1:c.7T>C	ENSP00000387919.2:p.Cys3Arg
ENST00000474397.5:c.7T>C	ENSP00000471271.1:p.Cys3Arg
ENST00000479081.5:c.7T>C	ENSP00000471544.1:p.Cys3Arg
NM_001316329.1:c.391T>C	NP_001303258.1:p.Cys131Arg
NM_002739.3:c.391T>C , LRG_669t1:c.391T>C	NP_002730.1:p.Cys131Arg
NM_002739.4:c.391T>C	NP_002730.1:p.Cys131Arg
NM_002739.5:c.391T>C MANE Select	NP_002730.1:p.Cys131Arg
NM_001316329.2:c.391T>C	NP_001303258.1:p.Cys131Arg