Canonical Allele Identifier: CA407414449

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 1184998
• ClinVar RCV Id: RCV001543622 ; RCV004526130
• dbSNP Id: rs1385053433
• MyVariant Identifiers: chr19:g.54393192C>G (hg19) ; chr19:g.53889938C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889938C>G , CM000681.2:g.53889938C>G	GRCh38
NC_000019.9:g.54393192C>G , CM000681.1:g.54393192C>G	GRCh37
NC_000019.8:g.59085004C>G	NCBI36
NG_009114.1:g.12726C>G , LRG_669:g.12726C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.450C>G	ENSP00000507230.1:p.Cys150Trp
ENST00000682268.1:n.748C>G
ENST00000682902.1:n.752C>G
ENST00000683513.1:c.450C>G	ENSP00000506809.1:p.Cys150Trp
ENST00000263431.4:c.450C>G MANE Select	ENSP00000263431.3:p.Cys150Trp
ENST00000263431.3:c.450C>G	ENSP00000263431.3:p.Cys150Trp
ENST00000419486.1:c.66C>G	ENSP00000387919.2:p.Cys22Trp
ENST00000474397.5:c.66C>G	ENSP00000471271.1:p.Cys22Trp
NM_001316329.1:c.450C>G	NP_001303258.1:p.Cys150Trp
NM_002739.3:c.450C>G , LRG_669t1:c.450C>G	NP_002730.1:p.Cys150Trp
NM_002739.4:c.450C>G	NP_002730.1:p.Cys150Trp
NM_002739.5:c.450C>G MANE Select	NP_002730.1:p.Cys150Trp
NM_001316329.2:c.450C>G	NP_001303258.1:p.Cys150Trp