Canonical Allele Identifier: CA508782877

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 1807563
• ClinVar RCV Id: RCV002475520
• dbSNP Id: rs147016991
• MyVariant Identifiers: chr19:g.54385847C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882593C>G , CM000681.2:g.53882593C>G	GRCh38
NC_000019.9:g.54385847C>G , CM000681.1:g.54385847C>G	GRCh37
NC_000019.8:g.59077659C>G	NCBI36
NG_009114.1:g.5381C>G , LRG_669:g.5381C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.99C>G	ENSP00000507230.1:p.Val33=
ENST00000682268.1:n.397C>G
ENST00000682902.1:n.401C>G
ENST00000683513.1:c.99C>G	ENSP00000506809.1:p.Val33=
ENST00000263431.4:c.99C>G MANE Select	ENSP00000263431.3:p.Val33=
ENST00000263431.3:c.99C>G	ENSP00000263431.3:p.Val33=
ENST00000419486.1:c.-286C>G	ENSP00000387919.2:n.-286C>G
ENST00000474397.5:c.-286C>G	ENSP00000471271.1:n.-286C>G
ENST00000479081.5:c.-286C>G	ENSP00000471544.1:n.-286C>G
NM_001316329.1:c.99C>G	NP_001303258.1:p.Val33=
NM_002739.3:c.99C>G , LRG_669t1:c.99C>G	NP_002730.1:p.Val33=
NM_002739.4:c.99C>G	NP_002730.1:p.Val33=
NM_002739.5:c.99C>G MANE Select	NP_002730.1:p.Val33=
NM_001316329.2:c.99C>G	NP_001303258.1:p.Val33=