Canonical Allele Identifier: CA2739629921

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882337C>G , CM000681.2:g.53882337C>G	GRCh38
NC_000019.9:g.54385591C>G , CM000681.1:g.54385591C>G	GRCh37
NC_000019.8:g.59077403C>G	NCBI36
NG_009114.1:g.5125C>G , LRG_669:g.5125C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-158C>G	ENSP00000507230.1:n.-158C>G
ENST00000682268.1:n.141C>G
ENST00000682902.1:n.145C>G
ENST00000683513.1:c.-158C>G	ENSP00000506809.1:n.-158C>G
ENST00000263431.4:c.-158C>G MANE Select	ENSP00000263431.3:n.-158C>G
ENST00000263431.3:c.-158C>G	ENSP00000263431.3:n.-158C>G
ENST00000419486.1:c.-345C>G	ENSP00000387919.2:n.-345C>G
ENST00000474397.5:c.-322-220C>G	ENSP00000471271.1:n.-322-220C>G
ENST00000479081.5:c.-322-220C>G	ENSP00000471544.1:n.-322-220C>G
NM_001316329.1:c.-158C>G	NP_001303258.1:n.-158C>G
NM_002739.3:c.-158C>G , LRG_669t1:c.-158C>G	NP_002730.1:n.-158C>G
NM_002739.4:c.-158C>G	NP_002730.1:n.-158C>G
NM_002739.5:c.-158C>G MANE Select	NP_002730.1:n.-158C>G
NM_001316329.2:c.-158C>G	NP_001303258.1:n.-158C>G