Canonical Allele Identifier: CA2342579275
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53889716T= , CM000681.2:g.53889716T= GRCh38
NC_000019.9:g.54392970T= , CM000681.1:g.54392970T= GRCh37
NC_000019.8:g.59084782T= NCBI36
NG_009114.1:g.12504T= , LRG_669:g.12504T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682028.1:c.364T= ENSP00000507230.1:p.Tyr122=
ENST00000682268.1:n.662T=
ENST00000682902.1:n.666T=
ENST00000683513.1:c.364T= ENSP00000506809.1:p.Tyr122=
ENST00000263431.4:c.364T= MANE Select ENSP00000263431.3:p.Tyr122=
ENST00000263431.3:c.364T= ENSP00000263431.3:p.Tyr122=
ENST00000419486.1:c.-21T= ENSP00000387919.2:n.-21T=
ENST00000474397.5:c.-21T= ENSP00000471271.1:n.-21T=
ENST00000479081.5:c.-21T= ENSP00000471544.1:n.-21T=
NM_001316329.1:c.364T= NP_001303258.1:p.Tyr122=
NM_002739.3:c.364T= , LRG_669t1:c.364T= NP_002730.1:p.Tyr122=
NM_002739.4:c.364T= NP_002730.1:p.Tyr122=
NM_002739.5:c.364T= MANE Select NP_002730.1:p.Tyr122=
NM_001316329.2:c.364T= NP_001303258.1:p.Tyr122=