Canonical Allele Identifier: CA344589

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 42132
• ClinVar RCV Id: RCV000034959
• dbSNP Id: rs386134158
• MyVariant Identifiers: chr19:g.54385870G>C (hg19) ; chr19:g.53882616G>C (hg38)
• PubMed: PMID:15824357 ; PMID:20301573

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882616G>C , CM000681.2:g.53882616G>C	GRCh38
NC_000019.9:g.54385870G>C , CM000681.1:g.54385870G>C	GRCh37
NC_000019.8:g.59077682G>C	NCBI36
NG_009114.1:g.5404G>C , LRG_669:g.5404G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.122G>C	ENSP00000507230.1:p.Arg41Pro
ENST00000682268.1:n.420G>C
ENST00000682902.1:n.424G>C
ENST00000683513.1:c.122G>C	ENSP00000506809.1:p.Arg41Pro
ENST00000263431.4:c.122G>C MANE Select	ENSP00000263431.3:p.Arg41Pro
ENST00000263431.3:c.122G>C	ENSP00000263431.3:p.Arg41Pro
ENST00000419486.1:c.-263G>C	ENSP00000387919.2:n.-263G>C
ENST00000474397.5:c.-263G>C	ENSP00000471271.1:n.-263G>C
ENST00000479081.5:c.-263G>C	ENSP00000471544.1:n.-263G>C
NM_001316329.1:c.122G>C	NP_001303258.1:p.Arg41Pro
NM_002739.3:c.122G>C , LRG_669t1:c.122G>C	NP_002730.1:p.Arg41Pro
NM_002739.4:c.122G>C	NP_002730.1:p.Arg41Pro
NM_002739.5:c.122G>C MANE Select	NP_002730.1:p.Arg41Pro
NM_001316329.2:c.122G>C	NP_001303258.1:p.Arg41Pro