Canonical Allele Identifier: CA344640

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 42169
• ClinVar RCV Id: RCV000034996 ; RCV000992818
• dbSNP Id: rs386134168
• MyVariant Identifiers: chr19:g.54393155T>A (hg19) ; chr19:g.53889901T>A (hg38)
• PubMed: PMID:16547918 ; PMID:20301573

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889901T>A , CM000681.2:g.53889901T>A	GRCh38
NC_000019.9:g.54393155T>A , CM000681.1:g.54393155T>A	GRCh37
NC_000019.8:g.59084967T>A	NCBI36
NG_009114.1:g.12689T>A , LRG_669:g.12689T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.413T>A	ENSP00000507230.1:p.Val138Glu
ENST00000682268.1:n.711T>A
ENST00000682902.1:n.715T>A
ENST00000683513.1:c.413T>A	ENSP00000506809.1:p.Val138Glu
ENST00000263431.4:c.413T>A MANE Select	ENSP00000263431.3:p.Val138Glu
ENST00000263431.3:c.413T>A	ENSP00000263431.3:p.Val138Glu
ENST00000419486.1:c.29T>A	ENSP00000387919.2:p.Val10Glu
ENST00000474397.5:c.29T>A	ENSP00000471271.1:p.Val10Glu
ENST00000479081.5:c.29T>A	ENSP00000471544.1:p.Val10Glu
NM_001316329.1:c.413T>A	NP_001303258.1:p.Val138Glu
NM_002739.3:c.413T>A , LRG_669t1:c.413T>A	NP_002730.1:p.Val138Glu
NM_002739.4:c.413T>A	NP_002730.1:p.Val138Glu
NM_002739.5:c.413T>A MANE Select	NP_002730.1:p.Val138Glu
NM_001316329.2:c.413T>A	NP_001303258.1:p.Val138Glu