Canonical Allele Identifier: CA9640141

Gene: PRKCG

Linked Data

• dbSNP Id: rs748380013
• ExAC: 19:54385559 C / G
• gnomAD v2: 19-54385559-C-G
• gnomAD v4: 19-53882305-C-G
• MyVariant Identifiers: chr19:g.54385559C>G (hg19) ; chr19:g.53882305C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882305C>G , CM000681.2:g.53882305C>G	GRCh38
NC_000019.9:g.54385559C>G , CM000681.1:g.54385559C>G	GRCh37
NC_000019.8:g.59077371C>G	NCBI36
NG_009114.1:g.5093C>G , LRG_669:g.5093C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-190C>G	ENSP00000507230.1:n.-190C>G
ENST00000682268.1:n.109C>G
ENST00000682902.1:n.113C>G
ENST00000683513.1:c.-190C>G	ENSP00000506809.1:n.-190C>G
ENST00000263431.4:c.-190C>G MANE Select	ENSP00000263431.3:n.-190C>G
ENST00000263431.3:c.-190C>G	ENSP00000263431.3:n.-190C>G
ENST00000419486.1:c.-377C>G	ENSP00000387919.2:n.-377C>G
ENST00000474397.5:c.-322-252C>G	ENSP00000471271.1:n.-322-252C>G
ENST00000479081.5:c.-322-252C>G	ENSP00000471544.1:n.-322-252C>G
NM_001316329.1:c.-190C>G	NP_001303258.1:n.-190C>G
NM_002739.3:c.-190C>G , LRG_669t1:c.-190C>G	NP_002730.1:n.-190C>G
NM_002739.4:c.-190C>G	NP_002730.1:n.-190C>G
NM_002739.5:c.-190C>G MANE Select	NP_002730.1:n.-190C>G
NM_001316329.2:c.-190C>G	NP_001303258.1:n.-190C>G