Canonical Allele Identifier: CA9640261

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 330059
• ClinVar RCV Id: RCV000407373
• dbSNP Id: rs143352499
• ExAC: 19:54392880 C / A
• gnomAD v2: 19-54392880-C-A
• gnomAD v3: 19-53889626-C-A
• gnomAD v4: 19-53889626-C-A
• MyVariant Identifiers: chr19:g.54392880C>A (hg19) ; chr19:g.53889626C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889626C>A , CM000681.2:g.53889626C>A	GRCh38
NC_000019.9:g.54392880C>A , CM000681.1:g.54392880C>A	GRCh37
NC_000019.8:g.59084692C>A	NCBI36
NG_009114.1:g.12414C>A , LRG_669:g.12414C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682028.1:c.286-12C>A	ENSP00000507230.1:n.286-12C>A
ENST00000682268.1:n.584-12C>A
ENST00000682902.1:n.588-12C>A
ENST00000683513.1:c.286-12C>A	ENSP00000506809.1:n.286-12C>A
ENST00000263431.4:c.286-12C>A MANE Select	ENSP00000263431.3:n.286-12C>A
ENST00000263431.3:c.286-12C>A	ENSP00000263431.3:n.286-12C>A
ENST00000419486.1:c.-99-12C>A	ENSP00000387919.2:n.-99-12C>A
ENST00000474397.5:c.-99-12C>A	ENSP00000471271.1:n.-99-12C>A
ENST00000479081.5:c.-99-12C>A	ENSP00000471544.1:n.-99-12C>A
NM_001316329.1:c.286-12C>A	NP_001303258.1:n.286-12C>A
NM_002739.3:c.286-12C>A , LRG_669t1:c.286-12C>A	NP_002730.1:n.286-12C>A
NM_002739.4:c.286-12C>A	NP_002730.1:n.286-12C>A
NM_002739.5:c.286-12C>A MANE Select	NP_002730.1:n.286-12C>A
NM_001316329.2:c.286-12C>A	NP_001303258.1:n.286-12C>A