Canonical Allele Identifier: CA2342579453

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890036_53890037delinsGC , CM000681.2:g.53890036_53890037delinsGC	GRCh38
NC_000019.9:g.54393290_54393291delinsGC , CM000681.1:g.54393290_54393291delinsGC	GRCh37
NC_000019.8:g.59085102_59085103delinsGC	NCBI36
NG_009114.1:g.12824_12825delinsGC , LRG_669:g.12824_12825delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+19_529+20delinsGC	ENSP00000507230.1:n.529+19_529+20delinsGC
ENST00000682268.1:n.827+19_827+20delinsGC
ENST00000682902.1:n.831+19_831+20delinsGC
ENST00000683513.1:c.529+19_529+20delinsGC	ENSP00000506809.1:n.529+19_529+20delinsGC
ENST00000263431.4:c.529+19_529+20delinsGC MANE Select	ENSP00000263431.3:n.529+19_529+20delinsGC
ENST00000263431.3:c.529+19_529+20delinsGC	ENSP00000263431.3:n.529+19_529+20delinsGC
ENST00000474397.5:c.145+19_145+20delinsGC	ENSP00000471271.1:n.145+19_145+20delinsGC
NM_001316329.1:c.529+19_529+20delinsGC	NP_001303258.1:n.529+19_529+20delinsGC
NM_002739.3:c.529+19_529+20delinsGC , LRG_669t1:c.529+19_529+20delinsGC	NP_002730.1:n.529+19_529+20delinsGC
NM_002739.4:c.529+19_529+20delinsGC	NP_002730.1:n.529+19_529+20delinsGC
NM_002739.5:c.529+19_529+20delinsGC MANE Select	NP_002730.1:n.529+19_529+20delinsGC
NM_001316329.2:c.529+19_529+20delinsGC	NP_001303258.1:n.529+19_529+20delinsGC