Canonical Allele Identifier: CA344584
Gene: PRKCG HGNC NCBI

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
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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
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