Canonical Allele Identifier: CA9640183
Gene: PRKCG HGNC NCBI

Linked Data

ClinVar Variation Id: 1045901
ClinVar RCV Id: RCV001350384
dbSNP Id: rs763526841

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882571G>A , CM000681.2:g.53882571G>A GRCh38
NC_000019.9:g.54385825G>A , CM000681.1:g.54385825G>A GRCh37
NC_000019.8:g.59077637G>A NCBI36
NG_009114.1:g.5359G>A , LRG_669:g.5359G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.77G>A ENSP00000507230.1:p.Arg26Lys
ENST00000682268.1:n.375G>A
ENST00000682902.1:n.379G>A
ENST00000683513.1:c.77G>A ENSP00000506809.1:p.Arg26Lys
ENST00000263431.4:c.77G>A MANE Select ENSP00000263431.3:p.Arg26Lys
ENST00000263431.3:c.77G>A ENSP00000263431.3:p.Arg26Lys
ENST00000419486.1:c.-308G>A ENSP00000387919.2:n.-308G>A
ENST00000474397.5:c.-308G>A ENSP00000471271.1:n.-308G>A
ENST00000479081.5:c.-308G>A ENSP00000471544.1:n.-308G>A
NM_001316329.1:c.77G>A NP_001303258.1:p.Arg26Lys
NM_002739.3:c.77G>A , LRG_669t1:c.77G>A NP_002730.1:p.Arg26Lys
NM_002739.4:c.77G>A NP_002730.1:p.Arg26Lys
NM_002739.5:c.77G>A MANE Select NP_002730.1:p.Arg26Lys
NM_001316329.2:c.77G>A NP_001303258.1:p.Arg26Lys