Canonical Allele Identifier: CA2342584713
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53900448T= , CM000681.2:g.53900448T= GRCh38
NC_000019.9:g.54403702T= , CM000681.1:g.54403702T= GRCh37
NC_000019.8:g.59095514T= NCBI36
NG_009114.1:g.23236T= , LRG_669:g.23236T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682028.1:c.1403T= ENSP00000507230.1:p.Leu468=
ENST00000682268.1:n.1701T=
ENST00000682676.1:n.804T=
ENST00000682902.1:n.1705T=
ENST00000683513.1:c.1403T= ENSP00000506809.1:p.Leu468=
ENST00000263431.4:c.1403T= MANE Select ENSP00000263431.3:p.Leu468=
ENST00000263431.3:c.1403T= ENSP00000263431.3:p.Leu468=
NM_001316329.1:c.1403T= NP_001303258.1:p.Leu468=
NM_002739.3:c.1403T= , LRG_669t1:c.1403T= NP_002730.1:p.Leu468=
NM_002739.4:c.1403T= NP_002730.1:p.Leu468=
XM_011527108.1:c.494T= XP_011525410.1:p.Leu165=
NM_002739.5:c.1403T= MANE Select NP_002730.1:p.Leu468=
NM_001316329.2:c.1403T= NP_001303258.1:p.Leu468=