Canonical Allele Identifier: CA2814830673

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889848_53889849insGGGGGG , CM000681.2:g.53889848_53889849insGGGGGG	GRCh38
NC_000019.9:g.54393102_54393103insGGGGGG , CM000681.1:g.54393102_54393103insGGGGGG	GRCh37
NC_000019.8:g.59084914_59084915insGGGGGG	NCBI36
NG_009114.1:g.12636_12637insGGGGGG , LRG_669:g.12636_12637insGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.398-38_398-37insGGGGGG	ENSP00000507230.1:n.398-38_398-37insGGGGGG
ENST00000682268.1:n.696-38_696-37insGGGGGG
ENST00000682902.1:n.700-38_700-37insGGGGGG
ENST00000683513.1:c.398-38_398-37insGGGGGG	ENSP00000506809.1:n.398-38_398-37insGGGGGG
ENST00000263431.4:c.398-38_398-37insGGGGGG MANE Select	ENSP00000263431.3:n.398-38_398-37insGGGGGG
ENST00000263431.3:c.398-38_398-37insGGGGGG	ENSP00000263431.3:n.398-38_398-37insGGGGGG
ENST00000419486.1:c.14-38_14-37insGGGGGG	ENSP00000387919.2:n.14-38_14-37insGGGGGG
ENST00000474397.5:c.14-38_14-37insGGGGGG	ENSP00000471271.1:n.14-38_14-37insGGGGGG
ENST00000479081.5:c.14-38_14-37insGGGGGG	ENSP00000471544.1:n.14-38_14-37insGGGGGG
NM_001316329.1:c.398-38_398-37insGGGGGG	NP_001303258.1:n.398-38_398-37insGGGGGG
NM_002739.3:c.398-38_398-37insGGGGGG , LRG_669t1:c.398-38_398-37insGGGGGG	NP_002730.1:n.398-38_398-37insGGGGGG
NM_002739.4:c.398-38_398-37insGGGGGG	NP_002730.1:n.398-38_398-37insGGGGGG
NM_002739.5:c.398-38_398-37insGGGGGG MANE Select	NP_002730.1:n.398-38_398-37insGGGGGG
NM_001316329.2:c.398-38_398-37insGGGGGG	NP_001303258.1:n.398-38_398-37insGGGGGG