Canonical Allele Identifier: CA2342584728

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900499T= , CM000681.2:g.53900499T=	GRCh38
NC_000019.9:g.54403753T= , CM000681.1:g.54403753T=	GRCh37
NC_000019.8:g.59095565T=	NCBI36
NG_009114.1:g.23287T= , LRG_669:g.23287T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1436+18T=	ENSP00000507230.1:n.1436+18T=
ENST00000682268.1:n.1734+18T=
ENST00000682676.1:n.837+18T=
ENST00000682902.1:n.1738+18T=
ENST00000683513.1:c.1436+18T=	ENSP00000506809.1:n.1436+18T=
ENST00000263431.4:c.1436+18T= MANE Select	ENSP00000263431.3:n.1436+18T=
ENST00000263431.3:c.1436+18T=	ENSP00000263431.3:n.1436+18T=
NM_001316329.1:c.1436+18T=	NP_001303258.1:n.1436+18T=
NM_002739.3:c.1436+18T= , LRG_669t1:c.1436+18T=	NP_002730.1:n.1436+18T=
NM_002739.4:c.1436+18T=	NP_002730.1:n.1436+18T=
XM_011527108.1:c.527+18T=	XP_011525410.1:n.527+18T=
NM_002739.5:c.1436+18T= MANE Select	NP_002730.1:n.1436+18T=
NM_001316329.2:c.1436+18T=	NP_001303258.1:n.1436+18T=