Canonical Allele Identifier: CA2342584880

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900875C= , CM000681.2:g.53900875C=	GRCh38
NC_000019.9:g.54404129C= , CM000681.1:g.54404129C=	GRCh37
NC_000019.8:g.59095941C=	NCBI36
NG_009114.1:g.23663C= , LRG_669:g.23663C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+126C=	ENSP00000507230.1:n.1575+126C=
ENST00000682268.1:n.1873+126C=
ENST00000682676.1:n.976+126C=
ENST00000682902.1:n.1877+126C=
ENST00000683513.1:c.1575+126C=	ENSP00000506809.1:n.1575+126C=
ENST00000263431.4:c.1575+126C= MANE Select	ENSP00000263431.3:n.1575+126C=
ENST00000263431.3:c.1575+126C=	ENSP00000263431.3:n.1575+126C=
NM_001316329.1:c.1575+126C=	NP_001303258.1:n.1575+126C=
NM_002739.3:c.1575+126C= , LRG_669t1:c.1575+126C=	NP_002730.1:n.1575+126C=
NM_002739.4:c.1575+126C=	NP_002730.1:n.1575+126C=
XM_011527108.1:c.666+126C=	XP_011525410.1:n.666+126C=
NM_002739.5:c.1575+126C= MANE Select	NP_002730.1:n.1575+126C=
NM_001316329.2:c.1575+126C=	NP_001303258.1:n.1575+126C=