Canonical Allele Identifier: CA344597

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 42140
• ClinVar RCV Id: RCV000034967 ; RCV001818213
• dbSNP Id: rs386134159
• MyVariant Identifiers: chr19:g.54386434G>T (hg19) ; chr19:g.53883180G>T (hg38)
• PubMed: PMID:17149711 ; PMID:20301573

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53883180G>T , CM000681.2:g.53883180G>T	GRCh38
NC_000019.9:g.54386434G>T , CM000681.1:g.54386434G>T	GRCh37
NC_000019.8:g.59078246G>T	NCBI36
NG_009114.1:g.5968G>T , LRG_669:g.5968G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.188G>T	ENSP00000507230.1:p.Gly63Val
ENST00000682268.1:n.486G>T
ENST00000682902.1:n.490G>T
ENST00000683513.1:c.188G>T	ENSP00000506809.1:p.Gly63Val
ENST00000263431.4:c.188G>T MANE Select	ENSP00000263431.3:p.Gly63Val
ENST00000263431.3:c.188G>T	ENSP00000263431.3:p.Gly63Val
ENST00000419486.1:c.-197G>T	ENSP00000387919.2:n.-197G>T
ENST00000474397.5:c.-197G>T	ENSP00000471271.1:n.-197G>T
ENST00000479081.5:c.-197G>T	ENSP00000471544.1:n.-197G>T
NM_001316329.1:c.188G>T	NP_001303258.1:p.Gly63Val
NM_002739.3:c.188G>T , LRG_669t1:c.188G>T	NP_002730.1:p.Gly63Val
NM_002739.4:c.188G>T	NP_002730.1:p.Gly63Val
NM_002739.5:c.188G>T MANE Select	NP_002730.1:p.Gly63Val
NM_001316329.2:c.188G>T	NP_001303258.1:p.Gly63Val