Canonical Allele Identifier: CA341272

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 13250
• ClinVar RCV Id: RCV001288717 ; RCV000014155
• dbSNP Id: rs121918517
• MyVariant Identifiers: chr19:g.54401354A>G (hg19) ; chr19:g.53898100A>G (hg38)
• PubMed: PMID:15824357 ; PMID:20301573

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53898100A>G , CM000681.2:g.53898100A>G	GRCh38
NC_000019.9:g.54401354A>G , CM000681.1:g.54401354A>G	GRCh37
NC_000019.8:g.59093166A>G	NCBI36
NG_009114.1:g.20888A>G , LRG_669:g.20888A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1081A>G	ENSP00000507230.1:p.Ser361Gly
ENST00000682268.1:n.1379A>G
ENST00000682676.1:n.482A>G
ENST00000682902.1:n.1383A>G
ENST00000683513.1:c.1081A>G	ENSP00000506809.1:p.Ser361Gly
ENST00000263431.4:c.1081A>G MANE Select	ENSP00000263431.3:p.Ser361Gly
ENST00000263431.3:c.1081A>G	ENSP00000263431.3:p.Ser361Gly
NM_001316329.1:c.1081A>G	NP_001303258.1:p.Ser361Gly
NM_002739.3:c.1081A>G , LRG_669t1:c.1081A>G	NP_002730.1:p.Ser361Gly
NM_002739.4:c.1081A>G	NP_002730.1:p.Ser361Gly
XM_011527108.1:c.172A>G	XP_011525410.1:p.Ser58Gly
NM_002739.5:c.1081A>G MANE Select	NP_002730.1:p.Ser361Gly
NM_001316329.2:c.1081A>G	NP_001303258.1:p.Ser361Gly