Canonical Allele Identifier: CA2814830677

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890066_53890067insGGG , CM000681.2:g.53890066_53890067insGGG	GRCh38
NC_000019.9:g.54393320_54393321insGGG , CM000681.1:g.54393320_54393321insGGG	GRCh37
NC_000019.8:g.59085132_59085133insGGG	NCBI36
NG_009114.1:g.12854_12855insGGG , LRG_669:g.12854_12855insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+49_529+50insGGG	ENSP00000507230.1:n.529+49_529+50insGGG
ENST00000682268.1:n.827+49_827+50insGGG
ENST00000682902.1:n.831+49_831+50insGGG
ENST00000683513.1:c.529+49_529+50insGGG	ENSP00000506809.1:n.529+49_529+50insGGG
ENST00000263431.4:c.529+49_529+50insGGG MANE Select	ENSP00000263431.3:n.529+49_529+50insGGG
ENST00000263431.3:c.529+49_529+50insGGG	ENSP00000263431.3:n.529+49_529+50insGGG
ENST00000474397.5:c.145+49_145+50insGGG	ENSP00000471271.1:n.145+49_145+50insGGG
NM_001316329.1:c.529+49_529+50insGGG	NP_001303258.1:n.529+49_529+50insGGG
NM_002739.3:c.529+49_529+50insGGG , LRG_669t1:c.529+49_529+50insGGG	NP_002730.1:n.529+49_529+50insGGG
NM_002739.4:c.529+49_529+50insGGG	NP_002730.1:n.529+49_529+50insGGG
NM_002739.5:c.529+49_529+50insGGG MANE Select	NP_002730.1:n.529+49_529+50insGGG
NM_001316329.2:c.529+49_529+50insGGG	NP_001303258.1:n.529+49_529+50insGGG