Canonical Allele Identifier: CA310082463

Gene: PRKCG

Linked Data

• dbSNP Id: rs943358171
• gnomAD v4: 19-53889538-T-A
• MyVariant Identifiers: chr19:g.54392792T>A (hg19) ; chr19:g.53889538T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889538T>A , CM000681.2:g.53889538T>A	GRCh38
NC_000019.9:g.54392792T>A , CM000681.1:g.54392792T>A	GRCh37
NC_000019.8:g.59084604T>A	NCBI36
NG_009114.1:g.12326T>A , LRG_669:g.12326T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.286-100T>A	ENSP00000507230.1:n.286-100T>A
ENST00000682268.1:n.584-100T>A
ENST00000682902.1:n.588-100T>A
ENST00000683513.1:c.286-100T>A	ENSP00000506809.1:n.286-100T>A
ENST00000263431.4:c.286-100T>A MANE Select	ENSP00000263431.3:n.286-100T>A
ENST00000263431.3:c.286-100T>A	ENSP00000263431.3:n.286-100T>A
ENST00000419486.1:c.-99-100T>A	ENSP00000387919.2:n.-99-100T>A
ENST00000474397.5:c.-99-100T>A	ENSP00000471271.1:n.-99-100T>A
ENST00000479081.5:c.-99-100T>A	ENSP00000471544.1:n.-99-100T>A
NM_001316329.1:c.286-100T>A	NP_001303258.1:n.286-100T>A
NM_002739.3:c.286-100T>A , LRG_669t1:c.286-100T>A	NP_002730.1:n.286-100T>A
NM_002739.4:c.286-100T>A	NP_002730.1:n.286-100T>A
NM_002739.5:c.286-100T>A MANE Select	NP_002730.1:n.286-100T>A
NM_001316329.2:c.286-100T>A	NP_001303258.1:n.286-100T>A