Canonical Allele Identifier: CA2814831057

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900290_53900291insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT , CM000681.2:g.53900290_53900291insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT	GRCh38
NC_000019.9:g.54403544_54403545insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT , CM000681.1:g.54403544_54403545insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT	GRCh37
NC_000019.8:g.59095356_59095357insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT	NCBI36
NG_009114.1:g.23078_23079insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT , LRG_669:g.23078_23079insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1339_1340insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT	ENSP00000507230.1:p.Gln447ProfsTer?
ENST00000682268.1:n.1637_1638insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT
ENST00000682676.1:n.740_741insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT
ENST00000682902.1:n.1641_1642insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT
ENST00000683513.1:c.1339_1340insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT	ENSP00000506809.1:p.Gln447ProfsTer?
ENST00000263431.4:c.1339_1340insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT MANE Select	ENSP00000263431.3:p.Gln447ProfsTer?
ENST00000263431.3:c.1339_1340insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT	ENSP00000263431.3:p.Gln447ProfsTer?
NM_001316329.1:c.1339_1340insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT	NP_001303258.1:p.Gln447ProfsTer?
NM_002739.3:c.1339_1340insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT , LRG_669t1:c.1339_1340insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT	NP_002730.1:p.Gln447ProfsTer?
NM_002739.4:c.1339_1340insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT	NP_002730.1:p.Gln447ProfsTer?
XM_011527108.1:c.430_431insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT	XP_011525410.1:p.Gln144ProfsTer?
NM_002739.5:c.1339_1340insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT MANE Select	NP_002730.1:p.Gln447ProfsTer?
NM_001316329.2:c.1339_1340insCCACGTCTGTCCTGAGTGATCAGGAAAGAAATTCTCCT	NP_001303258.1:p.Gln447ProfsTer?