Canonical Allele Identifier: CA2342579231

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889608G= , CM000681.2:g.53889608G=	GRCh38
NC_000019.9:g.54392862G= , CM000681.1:g.54392862G=	GRCh37
NC_000019.8:g.59084674G=	NCBI36
NG_009114.1:g.12396G= , LRG_669:g.12396G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682028.1:c.286-30G=	ENSP00000507230.1:n.286-30G=
ENST00000682268.1:n.584-30G=
ENST00000682902.1:n.588-30G=
ENST00000683513.1:c.286-30G=	ENSP00000506809.1:n.286-30G=
ENST00000263431.4:c.286-30G= MANE Select	ENSP00000263431.3:n.286-30G=
ENST00000263431.3:c.286-30G=	ENSP00000263431.3:n.286-30G=
ENST00000419486.1:c.-99-30G=	ENSP00000387919.2:n.-99-30G=
ENST00000474397.5:c.-99-30G=	ENSP00000471271.1:n.-99-30G=
ENST00000479081.5:c.-99-30G=	ENSP00000471544.1:n.-99-30G=
NM_001316329.1:c.286-30G=	NP_001303258.1:n.286-30G=
NM_002739.3:c.286-30G= , LRG_669t1:c.286-30G=	NP_002730.1:n.286-30G=
NM_002739.4:c.286-30G=	NP_002730.1:n.286-30G=
NM_002739.5:c.286-30G= MANE Select	NP_002730.1:n.286-30G=
NM_001316329.2:c.286-30G=	NP_001303258.1:n.286-30G=