Canonical Allele Identifier: CA2697547258

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 2684342
• ClinVar RCV Id: RCV003482838

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882564_53882566delinsCCT , CM000681.2:g.53882564_53882566delinsCCT	GRCh38
NC_000019.9:g.54385818_54385820delinsCCT , CM000681.1:g.54385818_54385820delinsCCT	GRCh37
NC_000019.8:g.59077630_59077632delinsCCT	NCBI36
NG_009114.1:g.5352_5354delinsCCT , LRG_669:g.5352_5354delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.70_72delinsCCT	ENSP00000507230.1:p.Ala24Pro
ENST00000682268.1:n.368_370delinsCCT
ENST00000682902.1:n.372_374delinsCCT
ENST00000683513.1:c.70_72delinsCCT	ENSP00000506809.1:p.Ala24Pro
ENST00000263431.4:c.70_72delinsCCT MANE Select	ENSP00000263431.3:p.Ala24Pro
ENST00000263431.3:c.70_72delinsCCT	ENSP00000263431.3:p.Ala24Pro
ENST00000419486.1:c.-315_-313delinsCCT	ENSP00000387919.2:n.-315_-313delinsCCT
ENST00000474397.5:c.-315_-313delinsCCT	ENSP00000471271.1:n.-315_-313delinsCCT
ENST00000479081.5:c.-315_-313delinsCCT	ENSP00000471544.1:n.-315_-313delinsCCT
NM_001316329.1:c.70_72delinsCCT	NP_001303258.1:p.Ala24Pro
NM_002739.3:c.70_72delinsCCT , LRG_669t1:c.70_72delinsCCT	NP_002730.1:p.Ala24Pro
NM_002739.4:c.70_72delinsCCT	NP_002730.1:p.Ala24Pro
NM_002739.5:c.70_72delinsCCT MANE Select	NP_002730.1:p.Ala24Pro
NM_001316329.2:c.70_72delinsCCT	NP_001303258.1:p.Ala24Pro