Canonical Allele Identifier: CA407417616

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 448124
• ClinVar RCV Id: RCV000517423
• dbSNP Id: rs121918517
• COSMIC: COSM1222032
• MyVariant Identifiers: chr19:g.54401354A>C (hg19) ; chr19:g.53898100A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53898100A>C , CM000681.2:g.53898100A>C	GRCh38
NC_000019.9:g.54401354A>C , CM000681.1:g.54401354A>C	GRCh37
NC_000019.8:g.59093166A>C	NCBI36
NG_009114.1:g.20888A>C , LRG_669:g.20888A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682028.1:c.1081A>C	ENSP00000507230.1:p.Ser361Arg
ENST00000682268.1:n.1379A>C
ENST00000682676.1:n.482A>C
ENST00000682902.1:n.1383A>C
ENST00000683513.1:c.1081A>C	ENSP00000506809.1:p.Ser361Arg
ENST00000263431.4:c.1081A>C MANE Select	ENSP00000263431.3:p.Ser361Arg
ENST00000263431.3:c.1081A>C	ENSP00000263431.3:p.Ser361Arg
NM_001316329.1:c.1081A>C	NP_001303258.1:p.Ser361Arg
NM_002739.3:c.1081A>C , LRG_669t1:c.1081A>C	NP_002730.1:p.Ser361Arg
NM_002739.4:c.1081A>C	NP_002730.1:p.Ser361Arg
XM_011527108.1:c.172A>C	XP_011525410.1:p.Ser58Arg
NM_002739.5:c.1081A>C MANE Select	NP_002730.1:p.Ser361Arg
NM_001316329.2:c.1081A>C	NP_001303258.1:p.Ser361Arg