Canonical Allele Identifier: CA344650
Gene: PRKCG HGNC NCBI

Linked Data

ClinVar Variation Id: 42174
ClinVar RCV Id: RCV000035003
dbSNP Id: rs386134157

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882570A>G , CM000681.2:g.53882570A>G GRCh38
NC_000019.9:g.54385824A>G , CM000681.1:g.54385824A>G GRCh37
NC_000019.8:g.59077636A>G NCBI36
NG_009114.1:g.5358A>G , LRG_669:g.5358A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.76A>G ENSP00000507230.1:p.Arg26Gly
ENST00000682268.1:n.374A>G
ENST00000682902.1:n.378A>G
ENST00000683513.1:c.76A>G ENSP00000506809.1:p.Arg26Gly
ENST00000263431.4:c.76A>G MANE Select ENSP00000263431.3:p.Arg26Gly
ENST00000263431.3:c.76A>G ENSP00000263431.3:p.Arg26Gly
ENST00000419486.1:c.-309A>G ENSP00000387919.2:n.-309A>G
ENST00000474397.5:c.-309A>G ENSP00000471271.1:n.-309A>G
ENST00000479081.5:c.-309A>G ENSP00000471544.1:n.-309A>G
NM_001316329.1:c.76A>G NP_001303258.1:p.Arg26Gly
NM_002739.3:c.76A>G , LRG_669t1:c.76A>G NP_002730.1:p.Arg26Gly
NM_002739.4:c.76A>G NP_002730.1:p.Arg26Gly
NM_002739.5:c.76A>G MANE Select NP_002730.1:p.Arg26Gly
NM_001316329.2:c.76A>G NP_001303258.1:p.Arg26Gly