Canonical Allele Identifier: CA2342575816
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882287C= , CM000681.2:g.53882287C= GRCh38
NC_000019.9:g.54385541C= , CM000681.1:g.54385541C= GRCh37
NC_000019.8:g.59077353C= NCBI36
NG_009114.1:g.5075C= , LRG_669:g.5075C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-208C= ENSP00000507230.1:n.-208C=
ENST00000682268.1:n.91C=
ENST00000682902.1:n.95C=
ENST00000683513.1:c.-208C= ENSP00000506809.1:n.-208C=
ENST00000263431.4:c.-208C= MANE Select ENSP00000263431.3:n.-208C=
ENST00000263431.3:c.-208C= ENSP00000263431.3:n.-208C=
ENST00000419486.1:c.-395C= ENSP00000387919.2:n.-395C=
ENST00000474397.5:c.-322-270C= ENSP00000471271.1:n.-322-270C=
ENST00000479081.5:c.-322-270C= ENSP00000471544.1:n.-322-270C=
NM_001316329.1:c.-208C= NP_001303258.1:n.-208C=
NM_002739.3:c.-208C= , LRG_669t1:c.-208C= NP_002730.1:n.-208C=
NM_002739.4:c.-208C= NP_002730.1:n.-208C=
NM_002739.5:c.-208C= MANE Select NP_002730.1:n.-208C=
NM_001316329.2:c.-208C= NP_001303258.1:n.-208C=