Canonical Allele Identifier: CA407414505

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 805318
• ClinVar RCV Id: RCV000992820
• dbSNP Id: rs1599943390
• gnomAD v4: 19-53889964-G-A
• MyVariant Identifiers: chr19:g.54393218G>A (hg19) ; chr19:g.53889964G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889964G>A , CM000681.2:g.53889964G>A	GRCh38
NC_000019.9:g.54393218G>A , CM000681.1:g.54393218G>A	GRCh37
NC_000019.8:g.59085030G>A	NCBI36
NG_009114.1:g.12752G>A , LRG_669:g.12752G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.476G>A	ENSP00000507230.1:p.Gly159Glu
ENST00000682268.1:n.774G>A
ENST00000682902.1:n.778G>A
ENST00000683513.1:c.476G>A	ENSP00000506809.1:p.Gly159Glu
ENST00000263431.4:c.476G>A MANE Select	ENSP00000263431.3:p.Gly159Glu
ENST00000263431.3:c.476G>A	ENSP00000263431.3:p.Gly159Glu
ENST00000419486.1:c.92G>A	ENSP00000387919.2:p.Gly31Glu
ENST00000474397.5:c.92G>A	ENSP00000471271.1:p.Gly31Glu
NM_001316329.1:c.476G>A	NP_001303258.1:p.Gly159Glu
NM_002739.3:c.476G>A , LRG_669t1:c.476G>A	NP_002730.1:p.Gly159Glu
NM_002739.4:c.476G>A	NP_002730.1:p.Gly159Glu
NM_002739.5:c.476G>A MANE Select	NP_002730.1:p.Gly159Glu
NM_001316329.2:c.476G>A	NP_001303258.1:p.Gly159Glu