Canonical Allele Identifier: CA407414504
Gene: PRKCG HGNC NCBI

Linked Data

ClinVar Variation Id: 1708844
ClinVar RCV Id: RCV002288128

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53889963G>C , CM000681.2:g.53889963G>C GRCh38
NC_000019.9:g.54393217G>C , CM000681.1:g.54393217G>C GRCh37
NC_000019.8:g.59085029G>C NCBI36
NG_009114.1:g.12751G>C , LRG_669:g.12751G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.475G>C ENSP00000507230.1:p.Gly159Arg
ENST00000682268.1:n.773G>C
ENST00000682902.1:n.777G>C
ENST00000683513.1:c.475G>C ENSP00000506809.1:p.Gly159Arg
ENST00000263431.4:c.475G>C MANE Select ENSP00000263431.3:p.Gly159Arg
ENST00000263431.3:c.475G>C ENSP00000263431.3:p.Gly159Arg
ENST00000419486.1:c.91G>C ENSP00000387919.2:p.Gly31Arg
ENST00000474397.5:c.91G>C ENSP00000471271.1:p.Gly31Arg
NM_001316329.1:c.475G>C NP_001303258.1:p.Gly159Arg
NM_002739.3:c.475G>C , LRG_669t1:c.475G>C NP_002730.1:p.Gly159Arg
NM_002739.4:c.475G>C NP_002730.1:p.Gly159Arg
NM_002739.5:c.475G>C MANE Select NP_002730.1:p.Gly159Arg
NM_001316329.2:c.475G>C NP_001303258.1:p.Gly159Arg