Canonical Allele Identifier: CA344584

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 42129
• ClinVar RCV Id: RCV000034956
• dbSNP Id: rs386134171
• MyVariant Identifiers: chr19:g.54401351G>A (hg19) ; chr19:g.53898097G>A (hg38)
• PubMed: PMID:16193476 ; PMID:20301573

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53898097G>A , CM000681.2:g.53898097G>A	GRCh38
NC_000019.9:g.54401351G>A , CM000681.1:g.54401351G>A	GRCh37
NC_000019.8:g.59093163G>A	NCBI36
NG_009114.1:g.20885G>A , LRG_669:g.20885G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1078G>A	ENSP00000507230.1:p.Gly360Ser
ENST00000682268.1:n.1376G>A
ENST00000682676.1:n.479G>A
ENST00000682902.1:n.1380G>A
ENST00000683513.1:c.1078G>A	ENSP00000506809.1:p.Gly360Ser
ENST00000263431.4:c.1078G>A MANE Select	ENSP00000263431.3:p.Gly360Ser
ENST00000263431.3:c.1078G>A	ENSP00000263431.3:p.Gly360Ser
NM_001316329.1:c.1078G>A	NP_001303258.1:p.Gly360Ser
NM_002739.3:c.1078G>A , LRG_669t1:c.1078G>A	NP_002730.1:p.Gly360Ser
NM_002739.4:c.1078G>A	NP_002730.1:p.Gly360Ser
XM_011527108.1:c.169G>A	XP_011525410.1:p.Gly57Ser
NM_002739.5:c.1078G>A MANE Select	NP_002730.1:p.Gly360Ser
NM_001316329.2:c.1078G>A	NP_001303258.1:p.Gly360Ser