Canonical Allele Identifier: CA407414443

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 805317
• ClinVar RCV Id: RCV000992819
• dbSNP Id: rs1599943341
• MyVariant Identifiers: chr19:g.54393190T>C (hg19) ; chr19:g.53889936T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889936T>C , CM000681.2:g.53889936T>C	GRCh38
NC_000019.9:g.54393190T>C , CM000681.1:g.54393190T>C	GRCh37
NC_000019.8:g.59085002T>C	NCBI36
NG_009114.1:g.12724T>C , LRG_669:g.12724T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.448T>C	ENSP00000507230.1:p.Cys150Arg
ENST00000682268.1:n.746T>C
ENST00000682902.1:n.750T>C
ENST00000683513.1:c.448T>C	ENSP00000506809.1:p.Cys150Arg
ENST00000263431.4:c.448T>C MANE Select	ENSP00000263431.3:p.Cys150Arg
ENST00000263431.3:c.448T>C	ENSP00000263431.3:p.Cys150Arg
ENST00000419486.1:c.64T>C	ENSP00000387919.2:p.Cys22Arg
ENST00000474397.5:c.64T>C	ENSP00000471271.1:p.Cys22Arg
NM_001316329.1:c.448T>C	NP_001303258.1:p.Cys150Arg
NM_002739.3:c.448T>C , LRG_669t1:c.448T>C	NP_002730.1:p.Cys150Arg
NM_002739.4:c.448T>C	NP_002730.1:p.Cys150Arg
NM_002739.5:c.448T>C MANE Select	NP_002730.1:p.Cys150Arg
NM_001316329.2:c.448T>C	NP_001303258.1:p.Cys150Arg