Canonical Allele Identifier: CA2739629882

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882275T>A , CM000681.2:g.53882275T>A	GRCh38
NC_000019.9:g.54385529T>A , CM000681.1:g.54385529T>A	GRCh37
NC_000019.8:g.59077341T>A	NCBI36
NG_009114.1:g.5063T>A , LRG_669:g.5063T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-220T>A	ENSP00000507230.1:n.-220T>A
ENST00000682268.1:n.79T>A
ENST00000682902.1:n.83T>A
ENST00000683513.1:c.-220T>A	ENSP00000506809.1:n.-220T>A
ENST00000263431.4:c.-220T>A MANE Select	ENSP00000263431.3:n.-220T>A
ENST00000263431.3:c.-220T>A	ENSP00000263431.3:n.-220T>A
ENST00000419486.1:c.-407T>A	ENSP00000387919.2:n.-407T>A
ENST00000474397.5:c.-322-282T>A	ENSP00000471271.1:n.-322-282T>A
ENST00000479081.5:c.-322-282T>A	ENSP00000471544.1:n.-322-282T>A
NM_001316329.1:c.-220T>A	NP_001303258.1:n.-220T>A
NM_002739.3:c.-220T>A , LRG_669t1:c.-220T>A	NP_002730.1:n.-220T>A
NM_002739.4:c.-220T>A	NP_002730.1:n.-220T>A
NM_002739.5:c.-220T>A MANE Select	NP_002730.1:n.-220T>A
NM_001316329.2:c.-220T>A	NP_001303258.1:n.-220T>A