Canonical Allele Identifier: CA2342579415
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53889980G= , CM000681.2:g.53889980G= GRCh38
NC_000019.9:g.54393234G= , CM000681.1:g.54393234G= GRCh37
NC_000019.8:g.59085046G= NCBI36
NG_009114.1:g.12768G= , LRG_669:g.12768G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.492G= ENSP00000507230.1:p.Glu164=
ENST00000682268.1:n.790G=
ENST00000682902.1:n.794G=
ENST00000683513.1:c.492G= ENSP00000506809.1:p.Glu164=
ENST00000263431.4:c.492G= MANE Select ENSP00000263431.3:p.Glu164=
ENST00000263431.3:c.492G= ENSP00000263431.3:p.Glu164=
ENST00000474397.5:c.108G= ENSP00000471271.1:p.Glu36=
NM_001316329.1:c.492G= NP_001303258.1:p.Glu164=
NM_002739.3:c.492G= , LRG_669t1:c.492G= NP_002730.1:p.Glu164=
NM_002739.4:c.492G= NP_002730.1:p.Glu164=
NM_002739.5:c.492G= MANE Select NP_002730.1:p.Glu164=
NM_001316329.2:c.492G= NP_001303258.1:p.Glu164=