Canonical Allele Identifier: CA2586963391

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53889935-GTGCGGTGTGGACC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889936_53889948del , CM000681.2:g.53889936_53889948del	GRCh38
NC_000019.9:g.54393190_54393202del , CM000681.1:g.54393190_54393202del	GRCh37
NC_000019.8:g.59085002_59085014del	NCBI36
NG_009114.1:g.12724_12736del , LRG_669:g.12724_12736del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.448_460del	ENSP00000507230.1:p.Cys150ThrfsTer22
ENST00000682268.1:n.746_758del
ENST00000682902.1:n.750_762del
ENST00000683513.1:c.448_460del	ENSP00000506809.1:p.Cys150ThrfsTer22
ENST00000263431.4:c.448_460del MANE Select	ENSP00000263431.3:p.Cys150ThrfsTer22
ENST00000263431.3:c.448_460del	ENSP00000263431.3:p.Cys150ThrfsTer22
ENST00000419486.1:c.64_76del	ENSP00000387919.2:p.Cys22ThrfsTer?
ENST00000474397.5:c.64_76del	ENSP00000471271.1:p.Cys22ThrfsTer22
NM_001316329.1:c.448_460del	NP_001303258.1:p.Cys150ThrfsTer22
NM_002739.3:c.448_460del , LRG_669t1:c.448_460del	NP_002730.1:p.Cys150ThrfsTer22
NM_002739.4:c.448_460del	NP_002730.1:p.Cys150ThrfsTer22
NM_002739.5:c.448_460del MANE Select	NP_002730.1:p.Cys150ThrfsTer22
NM_001316329.2:c.448_460del	NP_001303258.1:p.Cys150ThrfsTer22