Canonical Allele Identifier: CA2342575867
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882355T= , CM000681.2:g.53882355T= GRCh38
NC_000019.9:g.54385609T= , CM000681.1:g.54385609T= GRCh37
NC_000019.8:g.59077421T= NCBI36
NG_009114.1:g.5143T= , LRG_669:g.5143T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-140T= ENSP00000507230.1:n.-140T=
ENST00000682268.1:n.159T=
ENST00000682902.1:n.163T=
ENST00000683513.1:c.-140T= ENSP00000506809.1:n.-140T=
ENST00000263431.4:c.-140T= MANE Select ENSP00000263431.3:n.-140T=
ENST00000263431.3:c.-140T= ENSP00000263431.3:n.-140T=
ENST00000419486.1:c.-327T= ENSP00000387919.2:n.-327T=
ENST00000474397.5:c.-322-202T= ENSP00000471271.1:n.-322-202T=
ENST00000479081.5:c.-322-202T= ENSP00000471544.1:n.-322-202T=
NM_001316329.1:c.-140T= NP_001303258.1:n.-140T=
NM_002739.3:c.-140T= , LRG_669t1:c.-140T= NP_002730.1:n.-140T=
NM_002739.4:c.-140T= NP_002730.1:n.-140T=
NM_002739.5:c.-140T= MANE Select NP_002730.1:n.-140T=
NM_001316329.2:c.-140T= NP_001303258.1:n.-140T=