Canonical Allele Identifier: CA407414545

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 586452
• ClinVar RCV Id: RCV000713009
• dbSNP Id: rs1252158483
• MyVariant Identifiers: chr19:g.54393237C>G (hg19) ; chr19:g.53889983C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889983C>G , CM000681.2:g.53889983C>G	GRCh38
NC_000019.9:g.54393237C>G , CM000681.1:g.54393237C>G	GRCh37
NC_000019.8:g.59085049C>G	NCBI36
NG_009114.1:g.12771C>G , LRG_669:g.12771C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.495C>G	ENSP00000507230.1:p.Ile165Met
ENST00000682268.1:n.793C>G
ENST00000682902.1:n.797C>G
ENST00000683513.1:c.495C>G	ENSP00000506809.1:p.Ile165Met
ENST00000263431.4:c.495C>G MANE Select	ENSP00000263431.3:p.Ile165Met
ENST00000263431.3:c.495C>G	ENSP00000263431.3:p.Ile165Met
ENST00000474397.5:c.111C>G	ENSP00000471271.1:p.Ile37Met
NM_001316329.1:c.495C>G	NP_001303258.1:p.Ile165Met
NM_002739.3:c.495C>G , LRG_669t1:c.495C>G	NP_002730.1:p.Ile165Met
NM_002739.4:c.495C>G	NP_002730.1:p.Ile165Met
NM_002739.5:c.495C>G MANE Select	NP_002730.1:p.Ile165Met
NM_001316329.2:c.495C>G	NP_001303258.1:p.Ile165Met