Canonical Allele Identifier: CA657433926

Gene: PRKCG

Linked Data

• COSMIC: COSN19704644

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882362dup , CM000681.2:g.53882362dup	GRCh38
NC_000019.9:g.54385616dup , CM000681.1:g.54385616dup	GRCh37
NC_000019.8:g.59077428dup	NCBI36
NG_009114.1:g.5150dup , LRG_669:g.5150dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-133dup	ENSP00000507230.1:n.-133dup
ENST00000682268.1:n.166dup
ENST00000682902.1:n.170dup
ENST00000683513.1:c.-133dup	ENSP00000506809.1:n.-133dup
ENST00000263431.4:c.-133dup MANE Select	ENSP00000263431.3:n.-133dup
ENST00000263431.3:c.-133dup	ENSP00000263431.3:n.-133dup
ENST00000419486.1:c.-323+3dup	ENSP00000387919.2:n.-323+3dup
ENST00000474397.5:c.-322-195dup	ENSP00000471271.1:n.-322-195dup
ENST00000479081.5:c.-322-195dup	ENSP00000471544.1:n.-322-195dup
NM_001316329.1:c.-133dup	NP_001303258.1:n.-133dup
NM_002739.3:c.-133dup , LRG_669t1:c.-133dup	NP_002730.1:n.-133dup
NM_002739.4:c.-133dup	NP_002730.1:n.-133dup
NM_002739.5:c.-133dup MANE Select	NP_002730.1:n.-133dup
NM_001316329.2:c.-133dup	NP_001303258.1:n.-133dup