Canonical Allele Identifier: CA225981
Gene: PRKCG HGNC NCBI

Linked Data

ClinVar Variation Id: 98513
ClinVar RCV Id: RCV000084804
dbSNP Id: rs367543211
ExAC: 19:54395883 G / A
gnomAD v2: 19-54395883-G-A
gnomAD v4: 19-53892629-G-A
MyVariant Identifiers: chr19:g.54395883G>A (hg19) chr19:g.53892629G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53892629G>A , CM000681.2:g.53892629G>A GRCh38
NC_000019.9:g.54395883G>A , CM000681.1:g.54395883G>A GRCh37
NC_000019.8:g.59087695G>A NCBI36
NG_009114.1:g.15417G>A , LRG_669:g.15417G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.807G>A ENSP00000507230.1:p.Ala269=
ENST00000682268.1:n.1105G>A
ENST00000682902.1:n.1109G>A
ENST00000683513.1:c.807G>A ENSP00000506809.1:p.Ala269=
ENST00000263431.4:c.807G>A MANE Select ENSP00000263431.3:p.Ala269=
ENST00000263431.3:c.807G>A ENSP00000263431.3:p.Ala269=
NM_001316329.1:c.807G>A NP_001303258.1:p.Ala269=
NM_002739.3:c.807G>A , LRG_669t1:c.807G>A NP_002730.1:p.Ala269=
NM_002739.4:c.807G>A NP_002730.1:p.Ala269=
NM_002739.5:c.807G>A MANE Select NP_002730.1:p.Ala269=
NM_001316329.2:c.807G>A NP_001303258.1:p.Ala269=
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