Canonical Allele Identifier: CA2342579405
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53889958G= , CM000681.2:g.53889958G= GRCh38
NC_000019.9:g.54393212G= , CM000681.1:g.54393212G= GRCh37
NC_000019.8:g.59085024G= NCBI36
NG_009114.1:g.12746G= , LRG_669:g.12746G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.470G= ENSP00000507230.1:p.Arg157=
ENST00000682268.1:n.768G=
ENST00000682902.1:n.772G=
ENST00000683513.1:c.470G= ENSP00000506809.1:p.Arg157=
ENST00000263431.4:c.470G= MANE Select ENSP00000263431.3:p.Arg157=
ENST00000263431.3:c.470G= ENSP00000263431.3:p.Arg157=
ENST00000419486.1:c.86G= ENSP00000387919.2:p.Arg29=
ENST00000474397.5:c.86G= ENSP00000471271.1:p.Arg29=
NM_001316329.1:c.470G= NP_001303258.1:p.Arg157=
NM_002739.3:c.470G= , LRG_669t1:c.470G= NP_002730.1:p.Arg157=
NM_002739.4:c.470G= NP_002730.1:p.Arg157=
NM_002739.5:c.470G= MANE Select NP_002730.1:p.Arg157=
NM_001316329.2:c.470G= NP_001303258.1:p.Arg157=