Canonical Allele Identifier: CA341257

Gene: PRKCG

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

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