Canonical Allele Identifier: CA341261

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 13246
• ClinVar RCV Id: RCV000014151
• dbSNP Id: rs121918513
• MyVariant Identifiers: chr19:g.54392989G>A (hg19) ; chr19:g.53889735G>A (hg38)
• PubMed: PMID:12644968 ; PMID:17024314 ; PMID:18986758 ; PMID:20301573

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889735G>A , CM000681.2:g.53889735G>A	GRCh38
NC_000019.9:g.54392989G>A , CM000681.1:g.54392989G>A	GRCh37
NC_000019.8:g.59084801G>A	NCBI36
NG_009114.1:g.12523G>A , LRG_669:g.12523G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.383G>A	ENSP00000507230.1:p.Gly128Asp
ENST00000682268.1:n.681G>A
ENST00000682902.1:n.685G>A
ENST00000683513.1:c.383G>A	ENSP00000506809.1:p.Gly128Asp
ENST00000263431.4:c.383G>A MANE Select	ENSP00000263431.3:p.Gly128Asp
ENST00000263431.3:c.383G>A	ENSP00000263431.3:p.Gly128Asp
ENST00000419486.1:c.-2G>A	ENSP00000387919.2:n.-2G>A
ENST00000474397.5:c.-2G>A	ENSP00000471271.1:n.-2G>A
ENST00000479081.5:c.-2G>A	ENSP00000471544.1:n.-2G>A
NM_001316329.1:c.383G>A	NP_001303258.1:p.Gly128Asp
NM_002739.3:c.383G>A , LRG_669t1:c.383G>A	NP_002730.1:p.Gly128Asp
NM_002739.4:c.383G>A	NP_002730.1:p.Gly128Asp
NM_002739.5:c.383G>A MANE Select	NP_002730.1:p.Gly128Asp
NM_001316329.2:c.383G>A	NP_001303258.1:p.Gly128Asp