Canonical Allele Identifier: CA2741640839

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889954_53889955insCAC , CM000681.2:g.53889954_53889955insCAC	GRCh38
NC_000019.9:g.54393208_54393209insCAC , CM000681.1:g.54393208_54393209insCAC	GRCh37
NC_000019.8:g.59085020_59085021insCAC	NCBI36
NG_009114.1:g.12742_12743insCAC , LRG_669:g.12742_12743insCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.466_467insCAC	ENSP00000507230.1:p.Glu156delinsAlaGln
ENST00000682268.1:n.764_765insCAC
ENST00000682902.1:n.768_769insCAC
ENST00000683513.1:c.466_467insCAC	ENSP00000506809.1:p.Glu156delinsAlaGln
ENST00000263431.4:c.466_467insCAC MANE Select	ENSP00000263431.3:p.Glu156delinsAlaGln
ENST00000263431.3:c.466_467insCAC	ENSP00000263431.3:p.Glu156delinsAlaGln
ENST00000419486.1:c.82_83insCAC	ENSP00000387919.2:p.Glu28delinsAlaGln
ENST00000474397.5:c.82_83insCAC	ENSP00000471271.1:p.Glu28delinsAlaGln
NM_001316329.1:c.466_467insCAC	NP_001303258.1:p.Glu156delinsAlaGln
NM_002739.3:c.466_467insCAC , LRG_669t1:c.466_467insCAC	NP_002730.1:p.Glu156delinsAlaGln
NM_002739.4:c.466_467insCAC	NP_002730.1:p.Glu156delinsAlaGln
NM_002739.5:c.466_467insCAC MANE Select	NP_002730.1:p.Glu156delinsAlaGln
NM_001316329.2:c.466_467insCAC	NP_001303258.1:p.Glu156delinsAlaGln