Canonical Allele Identifier: CA2342575983

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882593C= , CM000681.2:g.53882593C=	GRCh38
NC_000019.9:g.54385847C= , CM000681.1:g.54385847C=	GRCh37
NC_000019.8:g.59077659C=	NCBI36
NG_009114.1:g.5381C= , LRG_669:g.5381C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.99C=	ENSP00000507230.1:p.Val33=
ENST00000682268.1:n.397C=
ENST00000682902.1:n.401C=
ENST00000683513.1:c.99C=	ENSP00000506809.1:p.Val33=
ENST00000263431.4:c.99C= MANE Select	ENSP00000263431.3:p.Val33=
ENST00000263431.3:c.99C=	ENSP00000263431.3:p.Val33=
ENST00000419486.1:c.-286C=	ENSP00000387919.2:n.-286C=
ENST00000474397.5:c.-286C=	ENSP00000471271.1:n.-286C=
ENST00000479081.5:c.-286C=	ENSP00000471544.1:n.-286C=
NM_001316329.1:c.99C=	NP_001303258.1:p.Val33=
NM_002739.3:c.99C= , LRG_669t1:c.99C=	NP_002730.1:p.Val33=
NM_002739.4:c.99C=	NP_002730.1:p.Val33=
NM_002739.5:c.99C= MANE Select	NP_002730.1:p.Val33=
NM_001316329.2:c.99C=	NP_001303258.1:p.Val33=