Canonical Allele Identifier: CA2507445332

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882286A>G , CM000681.2:g.53882286A>G	GRCh38
NC_000019.9:g.54385540A>G , CM000681.1:g.54385540A>G	GRCh37
NC_000019.8:g.59077352A>G	NCBI36
NG_009114.1:g.5074A>G , LRG_669:g.5074A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-209A>G	ENSP00000507230.1:n.-209A>G
ENST00000682268.1:n.90A>G
ENST00000682902.1:n.94A>G
ENST00000683513.1:c.-209A>G	ENSP00000506809.1:n.-209A>G
ENST00000263431.4:c.-209A>G MANE Select	ENSP00000263431.3:n.-209A>G
ENST00000263431.3:c.-209A>G	ENSP00000263431.3:n.-209A>G
ENST00000419486.1:c.-396A>G	ENSP00000387919.2:n.-396A>G
ENST00000474397.5:c.-322-271A>G	ENSP00000471271.1:n.-322-271A>G
ENST00000479081.5:c.-322-271A>G	ENSP00000471544.1:n.-322-271A>G
NM_001316329.1:c.-209A>G	NP_001303258.1:n.-209A>G
NM_002739.3:c.-209A>G , LRG_669t1:c.-209A>G	NP_002730.1:n.-209A>G
NM_002739.4:c.-209A>G	NP_002730.1:n.-209A>G
NM_002739.5:c.-209A>G MANE Select	NP_002730.1:n.-209A>G
NM_001316329.2:c.-209A>G	NP_001303258.1:n.-209A>G