Canonical Allele Identifier: CA2342579448

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890033_53890034delinsCT , CM000681.2:g.53890033_53890034delinsCT	GRCh38
NC_000019.9:g.54393287_54393288delinsCT , CM000681.1:g.54393287_54393288delinsCT	GRCh37
NC_000019.8:g.59085099_59085100delinsCT	NCBI36
NG_009114.1:g.12821_12822delinsCT , LRG_669:g.12821_12822delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+16_529+17delinsCT	ENSP00000507230.1:n.529+16_529+17delinsCT
ENST00000682268.1:n.827+16_827+17delinsCT
ENST00000682902.1:n.831+16_831+17delinsCT
ENST00000683513.1:c.529+16_529+17delinsCT	ENSP00000506809.1:n.529+16_529+17delinsCT
ENST00000263431.4:c.529+16_529+17delinsCT MANE Select	ENSP00000263431.3:n.529+16_529+17delinsCT
ENST00000263431.3:c.529+16_529+17delinsCT	ENSP00000263431.3:n.529+16_529+17delinsCT
ENST00000474397.5:c.145+16_145+17delinsCT	ENSP00000471271.1:n.145+16_145+17delinsCT
NM_001316329.1:c.529+16_529+17delinsCT	NP_001303258.1:n.529+16_529+17delinsCT
NM_002739.3:c.529+16_529+17delinsCT , LRG_669t1:c.529+16_529+17delinsCT	NP_002730.1:n.529+16_529+17delinsCT
NM_002739.4:c.529+16_529+17delinsCT	NP_002730.1:n.529+16_529+17delinsCT
NM_002739.5:c.529+16_529+17delinsCT MANE Select	NP_002730.1:n.529+16_529+17delinsCT
NM_001316329.2:c.529+16_529+17delinsCT	NP_001303258.1:n.529+16_529+17delinsCT