Canonical Allele Identifier: CA2342584718

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900470C= , CM000681.2:g.53900470C=	GRCh38
NC_000019.9:g.54403724C= , CM000681.1:g.54403724C=	GRCh37
NC_000019.8:g.59095536C=	NCBI36
NG_009114.1:g.23258C= , LRG_669:g.23258C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1425C=	ENSP00000507230.1:p.Gly475=
ENST00000682268.1:n.1723C=
ENST00000682676.1:n.826C=
ENST00000682902.1:n.1727C=
ENST00000683513.1:c.1425C=	ENSP00000506809.1:p.Gly475=
ENST00000263431.4:c.1425C= MANE Select	ENSP00000263431.3:p.Gly475=
ENST00000263431.3:c.1425C=	ENSP00000263431.3:p.Gly475=
NM_001316329.1:c.1425C=	NP_001303258.1:p.Gly475=
NM_002739.3:c.1425C= , LRG_669t1:c.1425C=	NP_002730.1:p.Gly475=
NM_002739.4:c.1425C=	NP_002730.1:p.Gly475=
XM_011527108.1:c.516C=	XP_011525410.1:p.Gly172=
NM_002739.5:c.1425C= MANE Select	NP_002730.1:p.Gly475=
NM_001316329.2:c.1425C=	NP_001303258.1:p.Gly475=