Canonical Allele Identifier: CA2342575812

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882282C= , CM000681.2:g.53882282C=	GRCh38
NC_000019.9:g.54385536C= , CM000681.1:g.54385536C=	GRCh37
NC_000019.8:g.59077348C=	NCBI36
NG_009114.1:g.5070C= , LRG_669:g.5070C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-213C=	ENSP00000507230.1:n.-213C=
ENST00000682268.1:n.86C=
ENST00000682902.1:n.90C=
ENST00000683513.1:c.-213C=	ENSP00000506809.1:n.-213C=
ENST00000263431.4:c.-213C= MANE Select	ENSP00000263431.3:n.-213C=
ENST00000263431.3:c.-213C=	ENSP00000263431.3:n.-213C=
ENST00000419486.1:c.-400C=	ENSP00000387919.2:n.-400C=
ENST00000474397.5:c.-322-275C=	ENSP00000471271.1:n.-322-275C=
ENST00000479081.5:c.-322-275C=	ENSP00000471544.1:n.-322-275C=
NM_001316329.1:c.-213C=	NP_001303258.1:n.-213C=
NM_002739.3:c.-213C= , LRG_669t1:c.-213C=	NP_002730.1:n.-213C=
NM_002739.4:c.-213C=	NP_002730.1:n.-213C=
NM_002739.5:c.-213C= MANE Select	NP_002730.1:n.-213C=
NM_001316329.2:c.-213C=	NP_001303258.1:n.-213C=