Canonical Allele Identifier: CA344630
Gene: PRKCG HGNC NCBI

Linked Data

ClinVar Variation Id: 42165
ClinVar RCV Id: RCV000034992 RCV003886368
dbSNP Id: rs386134165
MyVariant Identifiers: chr19:g.54392974G>A (hg19) chr19:g.53889720G>A (hg38)
PubMed: PMID:16193476 PMID:20301573
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53889720G>A , CM000681.2:g.53889720G>A GRCh38
NC_000019.9:g.54392974G>A , CM000681.1:g.54392974G>A GRCh37
NC_000019.8:g.59084786G>A NCBI36
NG_009114.1:g.12508G>A , LRG_669:g.12508G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682028.1:c.368G>A ENSP00000507230.1:p.Gly123Glu
ENST00000682268.1:n.666G>A
ENST00000682902.1:n.670G>A
ENST00000683513.1:c.368G>A ENSP00000506809.1:p.Gly123Glu
ENST00000263431.4:c.368G>A MANE Select ENSP00000263431.3:p.Gly123Glu
ENST00000263431.3:c.368G>A ENSP00000263431.3:p.Gly123Glu
ENST00000419486.1:c.-17G>A ENSP00000387919.2:n.-17G>A
ENST00000474397.5:c.-17G>A ENSP00000471271.1:n.-17G>A
ENST00000479081.5:c.-17G>A ENSP00000471544.1:n.-17G>A
NM_001316329.1:c.368G>A NP_001303258.1:p.Gly123Glu
NM_002739.3:c.368G>A , LRG_669t1:c.368G>A NP_002730.1:p.Gly123Glu
NM_002739.4:c.368G>A NP_002730.1:p.Gly123Glu
NM_002739.5:c.368G>A MANE Select NP_002730.1:p.Gly123Glu
NM_001316329.2:c.368G>A NP_001303258.1:p.Gly123Glu
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