Canonical Allele Identifier: CA9640128

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 330055
• ClinVar RCV Id: RCV000279458
• dbSNP Id: rs752173466
• ExAC: 19:54385516 C / T
• gnomAD v2: 19-54385516-C-T
• gnomAD v3: 19-53882262-C-T
• gnomAD v4: 19-53882262-C-T
• MyVariant Identifiers: chr19:g.54385516C>T (hg19) ; chr19:g.53882262C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882262C>T , CM000681.2:g.53882262C>T	GRCh38
NC_000019.9:g.54385516C>T , CM000681.1:g.54385516C>T	GRCh37
NC_000019.8:g.59077328C>T	NCBI36
NG_009114.1:g.5050C>T , LRG_669:g.5050C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-233C>T	ENSP00000507230.1:n.-233C>T
ENST00000682268.1:n.66C>T
ENST00000682902.1:n.70C>T
ENST00000683513.1:c.-233C>T	ENSP00000506809.1:n.-233C>T
ENST00000263431.4:c.-233C>T MANE Select	ENSP00000263431.3:n.-233C>T
ENST00000263431.3:c.-233C>T	ENSP00000263431.3:n.-233C>T
ENST00000419486.1:c.-420C>T	ENSP00000387919.2:n.-420C>T
ENST00000474397.5:c.-322-295C>T	ENSP00000471271.1:n.-322-295C>T
ENST00000479081.5:c.-322-295C>T	ENSP00000471544.1:n.-322-295C>T
NM_001316329.1:c.-233C>T	NP_001303258.1:n.-233C>T
NM_002739.3:c.-233C>T , LRG_669t1:c.-233C>T	NP_002730.1:n.-233C>T
NM_002739.4:c.-233C>T	NP_002730.1:n.-233C>T
NM_002739.5:c.-233C>T MANE Select	NP_002730.1:n.-233C>T
NM_001316329.2:c.-233C>T	NP_001303258.1:n.-233C>T