Canonical Allele Identifier: CA2342579511

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890125_53890129delinsCTCTT , CM000681.2:g.53890125_53890129delinsCTCTT	GRCh38
NC_000019.9:g.54393379_54393383delinsCTCTT , CM000681.1:g.54393379_54393383delinsCTCTT	GRCh37
NC_000019.8:g.59085191_59085195delinsCTCTT	NCBI36
NG_009114.1:g.12913_12917delinsCTCTT , LRG_669:g.12913_12917delinsCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+108_529+112delinsCTCTT	ENSP00000507230.1:n.529+108_529+112delinsCTCTT
ENST00000682268.1:n.827+108_827+112delinsCTCTT
ENST00000682902.1:n.831+108_831+112delinsCTCTT
ENST00000683513.1:c.529+108_529+112delinsCTCTT	ENSP00000506809.1:n.529+108_529+112delinsCTCTT
ENST00000263431.4:c.529+108_529+112delinsCTCTT MANE Select	ENSP00000263431.3:n.529+108_529+112delinsCTCTT
ENST00000263431.3:c.529+108_529+112delinsCTCTT	ENSP00000263431.3:n.529+108_529+112delinsCTCTT
ENST00000474397.5:c.145+108_145+112delinsCTCTT	ENSP00000471271.1:n.145+108_145+112delinsCTCTT
NM_001316329.1:c.529+108_529+112delinsCTCTT	NP_001303258.1:n.529+108_529+112delinsCTCTT
NM_002739.3:c.529+108_529+112delinsCTCTT , LRG_669t1:c.529+108_529+112delinsCTCTT	NP_002730.1:n.529+108_529+112delinsCTCTT
NM_002739.4:c.529+108_529+112delinsCTCTT	NP_002730.1:n.529+108_529+112delinsCTCTT
NM_002739.5:c.529+108_529+112delinsCTCTT MANE Select	NP_002730.1:n.529+108_529+112delinsCTCTT
NM_001316329.2:c.529+108_529+112delinsCTCTT	NP_001303258.1:n.529+108_529+112delinsCTCTT