Canonical Allele Identifier: CA2342579512

Gene: PRKCG

Linked Data

• dbSNP Id: rs2068662660
• gnomAD v4: 19-53890125-CTCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890129_53890132del , CM000681.2:g.53890129_53890132del	GRCh38
NC_000019.9:g.54393383_54393386del , CM000681.1:g.54393383_54393386del	GRCh37
NC_000019.8:g.59085195_59085198del	NCBI36
NG_009114.1:g.12917_12920del , LRG_669:g.12917_12920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+112_529+115del	ENSP00000507230.1:n.529+112_529+115del
ENST00000682268.1:n.827+112_827+115del
ENST00000682902.1:n.831+112_831+115del
ENST00000683513.1:c.529+112_529+115del	ENSP00000506809.1:n.529+112_529+115del
ENST00000263431.4:c.529+112_529+115del MANE Select	ENSP00000263431.3:n.529+112_529+115del
ENST00000263431.3:c.529+112_529+115del	ENSP00000263431.3:n.529+112_529+115del
ENST00000474397.5:c.145+112_145+115del	ENSP00000471271.1:n.145+112_145+115del
NM_001316329.1:c.529+112_529+115del	NP_001303258.1:n.529+112_529+115del
NM_002739.3:c.529+112_529+115del , LRG_669t1:c.529+112_529+115del	NP_002730.1:n.529+112_529+115del
NM_002739.4:c.529+112_529+115del	NP_002730.1:n.529+112_529+115del
NM_002739.5:c.529+112_529+115del MANE Select	NP_002730.1:n.529+112_529+115del
NM_001316329.2:c.529+112_529+115del	NP_001303258.1:n.529+112_529+115del