Canonical Allele Identifier: CA2342575902

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882406T= , CM000681.2:g.53882406T=	GRCh38
NC_000019.9:g.54385660T= , CM000681.1:g.54385660T=	GRCh37
NC_000019.8:g.59077472T=	NCBI36
NG_009114.1:g.5194T= , LRG_669:g.5194T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-89T=	ENSP00000507230.1:n.-89T=
ENST00000682268.1:n.210T=
ENST00000682902.1:n.214T=
ENST00000683513.1:c.-89T=	ENSP00000506809.1:n.-89T=
ENST00000263431.4:c.-89T= MANE Select	ENSP00000263431.3:n.-89T=
ENST00000263431.3:c.-89T=	ENSP00000263431.3:n.-89T=
ENST00000419486.1:c.-323+47T=	ENSP00000387919.2:n.-323+47T=
ENST00000474397.5:c.-322-151T=	ENSP00000471271.1:n.-322-151T=
ENST00000479081.5:c.-322-151T=	ENSP00000471544.1:n.-322-151T=
NM_001316329.1:c.-89T=	NP_001303258.1:n.-89T=
NM_002739.3:c.-89T= , LRG_669t1:c.-89T=	NP_002730.1:n.-89T=
NM_002739.4:c.-89T=	NP_002730.1:n.-89T=
NM_002739.5:c.-89T= MANE Select	NP_002730.1:n.-89T=
NM_001316329.2:c.-89T=	NP_001303258.1:n.-89T=