Canonical Allele Identifier: CA2515966857

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900763_53900764insCC , CM000681.2:g.53900763_53900764insCC	GRCh38
NC_000019.9:g.54404017_54404018insCC , CM000681.1:g.54404017_54404018insCC	GRCh37
NC_000019.8:g.59095829_59095830insCC	NCBI36
NG_009114.1:g.23551_23552insCC , LRG_669:g.23551_23552insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+14_1575+15insCC	ENSP00000507230.1:n.1575+14_1575+15insCC
ENST00000682268.1:n.1873+14_1873+15insCC
ENST00000682676.1:n.976+14_976+15insCC
ENST00000682902.1:n.1877+14_1877+15insCC
ENST00000683513.1:c.1575+14_1575+15insCC	ENSP00000506809.1:n.1575+14_1575+15insCC
ENST00000263431.4:c.1575+14_1575+15insCC MANE Select	ENSP00000263431.3:n.1575+14_1575+15insCC
ENST00000263431.3:c.1575+14_1575+15insCC	ENSP00000263431.3:n.1575+14_1575+15insCC
NM_001316329.1:c.1575+14_1575+15insCC	NP_001303258.1:n.1575+14_1575+15insCC
NM_002739.3:c.1575+14_1575+15insCC , LRG_669t1:c.1575+14_1575+15insCC	NP_002730.1:n.1575+14_1575+15insCC
NM_002739.4:c.1575+14_1575+15insCC	NP_002730.1:n.1575+14_1575+15insCC
XM_011527108.1:c.666+14_666+15insCC	XP_011525410.1:n.666+14_666+15insCC
NM_002739.5:c.1575+14_1575+15insCC MANE Select	NP_002730.1:n.1575+14_1575+15insCC
NM_001316329.2:c.1575+14_1575+15insCC	NP_001303258.1:n.1575+14_1575+15insCC