Canonical Allele Identifier: CA2342575809

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882276_53882277delinsCT , CM000681.2:g.53882276_53882277delinsCT	GRCh38
NC_000019.9:g.54385530_54385531delinsCT , CM000681.1:g.54385530_54385531delinsCT	GRCh37
NC_000019.8:g.59077342_59077343delinsCT	NCBI36
NG_009114.1:g.5064_5065delinsCT , LRG_669:g.5064_5065delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-219_-218delinsCT	ENSP00000507230.1:n.-219_-218delinsCT
ENST00000682268.1:n.80_81delinsCT
ENST00000682902.1:n.84_85delinsCT
ENST00000683513.1:c.-219_-218delinsCT	ENSP00000506809.1:n.-219_-218delinsCT
ENST00000263431.4:c.-219_-218delinsCT MANE Select	ENSP00000263431.3:n.-219_-218delinsCT
ENST00000263431.3:c.-219_-218delinsCT	ENSP00000263431.3:n.-219_-218delinsCT
ENST00000419486.1:c.-406_-405delinsCT	ENSP00000387919.2:n.-406_-405delinsCT
ENST00000474397.5:c.-322-281_-322-280delinsCT	ENSP00000471271.1:n.-322-281_-322-280delinsCT
ENST00000479081.5:c.-322-281_-322-280delinsCT	ENSP00000471544.1:n.-322-281_-322-280delinsCT
NM_001316329.1:c.-219_-218delinsCT	NP_001303258.1:n.-219_-218delinsCT
NM_002739.3:c.-219_-218delinsCT , LRG_669t1:c.-219_-218delinsCT	NP_002730.1:n.-219_-218delinsCT
NM_002739.4:c.-219_-218delinsCT	NP_002730.1:n.-219_-218delinsCT
NM_002739.5:c.-219_-218delinsCT MANE Select	NP_002730.1:n.-219_-218delinsCT
NM_001316329.2:c.-219_-218delinsCT	NP_001303258.1:n.-219_-218delinsCT