Canonical Allele Identifier: CA2342575842
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882318C= , CM000681.2:g.53882318C= GRCh38
NC_000019.9:g.54385572C= , CM000681.1:g.54385572C= GRCh37
NC_000019.8:g.59077384C= NCBI36
NG_009114.1:g.5106C= , LRG_669:g.5106C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-177C= ENSP00000507230.1:n.-177C=
ENST00000682268.1:n.122C=
ENST00000682902.1:n.126C=
ENST00000683513.1:c.-177C= ENSP00000506809.1:n.-177C=
ENST00000263431.4:c.-177C= MANE Select ENSP00000263431.3:n.-177C=
ENST00000263431.3:c.-177C= ENSP00000263431.3:n.-177C=
ENST00000419486.1:c.-364C= ENSP00000387919.2:n.-364C=
ENST00000474397.5:c.-322-239C= ENSP00000471271.1:n.-322-239C=
ENST00000479081.5:c.-322-239C= ENSP00000471544.1:n.-322-239C=
NM_001316329.1:c.-177C= NP_001303258.1:n.-177C=
NM_002739.3:c.-177C= , LRG_669t1:c.-177C= NP_002730.1:n.-177C=
NM_002739.4:c.-177C= NP_002730.1:n.-177C=
NM_002739.5:c.-177C= MANE Select NP_002730.1:n.-177C=
NM_001316329.2:c.-177C= NP_001303258.1:n.-177C=