Canonical Allele Identifier: CA344608

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 42148
• ClinVar RCV Id: RCV000034975
• dbSNP Id: rs386134160
• MyVariant Identifiers: chr19:g.54387441T>A (hg19) ; chr19:g.53884187T>A (hg38)
• PubMed: PMID:17708558 ; PMID:20301573

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53884187T>A , CM000681.2:g.53884187T>A	GRCh38
NC_000019.9:g.54387441T>A , CM000681.1:g.54387441T>A	GRCh37
NC_000019.8:g.59079253T>A	NCBI36
NG_009114.1:g.6975T>A , LRG_669:g.6975T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.229T>A	ENSP00000507230.1:p.Cys77Ser
ENST00000682268.1:n.527T>A
ENST00000682902.1:n.531T>A
ENST00000683513.1:c.229T>A	ENSP00000506809.1:p.Cys77Ser
ENST00000263431.4:c.229T>A MANE Select	ENSP00000263431.3:p.Cys77Ser
ENST00000263431.3:c.229T>A	ENSP00000263431.3:p.Cys77Ser
ENST00000419486.1:c.-156T>A	ENSP00000387919.2:n.-156T>A
ENST00000474397.5:c.-156T>A	ENSP00000471271.1:n.-156T>A
ENST00000479081.5:c.-156T>A	ENSP00000471544.1:n.-156T>A
NM_001316329.1:c.229T>A	NP_001303258.1:p.Cys77Ser
NM_002739.3:c.229T>A , LRG_669t1:c.229T>A	NP_002730.1:p.Cys77Ser
NM_002739.4:c.229T>A	NP_002730.1:p.Cys77Ser
NM_002739.5:c.229T>A MANE Select	NP_002730.1:p.Cys77Ser
NM_001316329.2:c.229T>A	NP_001303258.1:p.Cys77Ser