Canonical Allele Identifier: CA2342575899
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882402C= , CM000681.2:g.53882402C= GRCh38
NC_000019.9:g.54385656C= , CM000681.1:g.54385656C= GRCh37
NC_000019.8:g.59077468C= NCBI36
NG_009114.1:g.5190C= , LRG_669:g.5190C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-93C= ENSP00000507230.1:n.-93C=
ENST00000682268.1:n.206C=
ENST00000682902.1:n.210C=
ENST00000683513.1:c.-93C= ENSP00000506809.1:n.-93C=
ENST00000263431.4:c.-93C= MANE Select ENSP00000263431.3:n.-93C=
ENST00000263431.3:c.-93C= ENSP00000263431.3:n.-93C=
ENST00000419486.1:c.-323+43C= ENSP00000387919.2:n.-323+43C=
ENST00000474397.5:c.-322-155C= ENSP00000471271.1:n.-322-155C=
ENST00000479081.5:c.-322-155C= ENSP00000471544.1:n.-322-155C=
NM_001316329.1:c.-93C= NP_001303258.1:n.-93C=
NM_002739.3:c.-93C= , LRG_669t1:c.-93C= NP_002730.1:n.-93C=
NM_002739.4:c.-93C= NP_002730.1:n.-93C=
NM_002739.5:c.-93C= MANE Select NP_002730.1:n.-93C=
NM_001316329.2:c.-93C= NP_001303258.1:n.-93C=