Canonical Allele Identifier: CA997083949

Gene: PRKCG

Linked Data

• dbSNP Id: rs2068752753
• gnomAD v3: 19-53900250-GA-G
• gnomAD v4: 19-53900250-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900251del , CM000681.2:g.53900251del	GRCh38
NC_000019.9:g.54403505del , CM000681.1:g.54403505del	GRCh37
NC_000019.8:g.59095317del	NCBI36
NG_009114.1:g.23039del , LRG_669:g.23039del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1300del	ENSP00000507230.1:p.Met434TrpfsTer9
ENST00000682268.1:n.1598del
ENST00000682676.1:n.701del
ENST00000682902.1:n.1602del
ENST00000683513.1:c.1300del	ENSP00000506809.1:p.Met434TrpfsTer9
ENST00000263431.4:c.1300del MANE Select	ENSP00000263431.3:p.Met434TrpfsTer9
ENST00000263431.3:c.1300del	ENSP00000263431.3:p.Met434TrpfsTer9
NM_001316329.1:c.1300del	NP_001303258.1:p.Met434TrpfsTer9
NM_002739.3:c.1300del , LRG_669t1:c.1300del	NP_002730.1:p.Met434TrpfsTer9
NM_002739.4:c.1300del	NP_002730.1:p.Met434TrpfsTer9
XM_011527108.1:c.391del	XP_011525410.1:p.Met131TrpfsTer9
NM_002739.5:c.1300del MANE Select	NP_002730.1:p.Met434TrpfsTer9
NM_001316329.2:c.1300del	NP_001303258.1:p.Met434TrpfsTer9