Canonical Allele Identifier: CA341257
Gene: PRKCG HGNC NCBI

Linked Data

ClinVar Variation Id: 13244
ClinVar RCV Id: RCV000014149 RCV001268861
dbSNP Id: rs121918511
MyVariant Identifiers: chr19:g.54392907C>T (hg19) chr19:g.53889653C>T (hg38)
PubMed: PMID:12164726 PMID:12644968 PMID:17659643 PMID:20301573
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53889653C>T , CM000681.2:g.53889653C>T GRCh38
NC_000019.9:g.54392907C>T , CM000681.1:g.54392907C>T GRCh37
NC_000019.8:g.59084719C>T NCBI36
NG_009114.1:g.12441C>T , LRG_669:g.12441C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682028.1:c.301C>T ENSP00000507230.1:p.His101Tyr
ENST00000682268.1:n.599C>T
ENST00000682902.1:n.603C>T
ENST00000683513.1:c.301C>T ENSP00000506809.1:p.His101Tyr
ENST00000263431.4:c.301C>T MANE Select ENSP00000263431.3:p.His101Tyr
ENST00000263431.3:c.301C>T ENSP00000263431.3:p.His101Tyr
ENST00000419486.1:c.-84C>T ENSP00000387919.2:n.-84C>T
ENST00000474397.5:c.-84C>T ENSP00000471271.1:n.-84C>T
ENST00000479081.5:c.-84C>T ENSP00000471544.1:n.-84C>T
NM_001316329.1:c.301C>T NP_001303258.1:p.His101Tyr
NM_002739.3:c.301C>T , LRG_669t1:c.301C>T NP_002730.1:p.His101Tyr
NM_002739.4:c.301C>T NP_002730.1:p.His101Tyr
NM_002739.5:c.301C>T MANE Select NP_002730.1:p.His101Tyr
NM_001316329.2:c.301C>T NP_001303258.1:p.His101Tyr
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