Canonical Allele Identifier: CA2576878525

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890062_53890063del , CM000681.2:g.53890062_53890063del	GRCh38
NC_000019.9:g.54393316_54393317del , CM000681.1:g.54393316_54393317del	GRCh37
NC_000019.8:g.59085128_59085129del	NCBI36
NG_009114.1:g.12850_12851del , LRG_669:g.12850_12851del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+45_529+46del	ENSP00000507230.1:n.529+45_529+46del
ENST00000682268.1:n.827+45_827+46del
ENST00000682902.1:n.831+45_831+46del
ENST00000683513.1:c.529+45_529+46del	ENSP00000506809.1:n.529+45_529+46del
ENST00000263431.4:c.529+45_529+46del MANE Select	ENSP00000263431.3:n.529+45_529+46del
ENST00000263431.3:c.529+45_529+46del	ENSP00000263431.3:n.529+45_529+46del
ENST00000474397.5:c.145+45_145+46del	ENSP00000471271.1:n.145+45_145+46del
NM_001316329.1:c.529+45_529+46del	NP_001303258.1:n.529+45_529+46del
NM_002739.3:c.529+45_529+46del , LRG_669t1:c.529+45_529+46del	NP_002730.1:n.529+45_529+46del
NM_002739.4:c.529+45_529+46del	NP_002730.1:n.529+45_529+46del
NM_002739.5:c.529+45_529+46del MANE Select	NP_002730.1:n.529+45_529+46del
NM_001316329.2:c.529+45_529+46del	NP_001303258.1:n.529+45_529+46del