Canonical Allele Identifier: CA2342575823
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882296_53882297delinsTC , CM000681.2:g.53882296_53882297delinsTC GRCh38
NC_000019.9:g.54385550_54385551delinsTC , CM000681.1:g.54385550_54385551delinsTC GRCh37
NC_000019.8:g.59077362_59077363delinsTC NCBI36
NG_009114.1:g.5084_5085delinsTC , LRG_669:g.5084_5085delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-199_-198delinsTC ENSP00000507230.1:n.-199_-198delinsTC
ENST00000682268.1:n.100_101delinsTC
ENST00000682902.1:n.104_105delinsTC
ENST00000683513.1:c.-199_-198delinsTC ENSP00000506809.1:n.-199_-198delinsTC
ENST00000263431.4:c.-199_-198delinsTC MANE Select ENSP00000263431.3:n.-199_-198delinsTC
ENST00000263431.3:c.-199_-198delinsTC ENSP00000263431.3:n.-199_-198delinsTC
ENST00000419486.1:c.-386_-385delinsTC ENSP00000387919.2:n.-386_-385delinsTC
ENST00000474397.5:c.-322-261_-322-260delinsTC ENSP00000471271.1:n.-322-261_-322-260delinsTC
ENST00000479081.5:c.-322-261_-322-260delinsTC ENSP00000471544.1:n.-322-261_-322-260delinsTC
NM_001316329.1:c.-199_-198delinsTC NP_001303258.1:n.-199_-198delinsTC
NM_002739.3:c.-199_-198delinsTC , LRG_669t1:c.-199_-198delinsTC NP_002730.1:n.-199_-198delinsTC
NM_002739.4:c.-199_-198delinsTC NP_002730.1:n.-199_-198delinsTC
NM_002739.5:c.-199_-198delinsTC MANE Select NP_002730.1:n.-199_-198delinsTC
NM_001316329.2:c.-199_-198delinsTC NP_001303258.1:n.-199_-198delinsTC