Canonical Allele Identifier: CA341263
Gene: PRKCG HGNC NCBI

Linked Data

ClinVar Variation Id: 13247
dbSNP Id: rs121918514

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53889705G>A , CM000681.2:g.53889705G>A GRCh38
NC_000019.9:g.54392959G>A , CM000681.1:g.54392959G>A GRCh37
NC_000019.8:g.59084771G>A NCBI36
NG_009114.1:g.12493G>A , LRG_669:g.12493G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682028.1:c.353G>A ENSP00000507230.1:p.Gly118Asp
ENST00000682268.1:n.651G>A
ENST00000682902.1:n.655G>A
ENST00000683513.1:c.353G>A ENSP00000506809.1:p.Gly118Asp
ENST00000263431.4:c.353G>A MANE Select ENSP00000263431.3:p.Gly118Asp
ENST00000263431.3:c.353G>A ENSP00000263431.3:p.Gly118Asp
ENST00000419486.1:c.-32G>A ENSP00000387919.2:n.-32G>A
ENST00000474397.5:c.-32G>A ENSP00000471271.1:n.-32G>A
ENST00000479081.5:c.-32G>A ENSP00000471544.1:n.-32G>A
NM_001316329.1:c.353G>A NP_001303258.1:p.Gly118Asp
NM_002739.3:c.353G>A , LRG_669t1:c.353G>A NP_002730.1:p.Gly118Asp
NM_002739.4:c.353G>A NP_002730.1:p.Gly118Asp
NM_002739.5:c.353G>A MANE Select NP_002730.1:p.Gly118Asp
NM_001316329.2:c.353G>A NP_001303258.1:p.Gly118Asp