Canonical Allele Identifier: CA891837658

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965377_87965379delinsTGT , CM000672.2:g.87965377_87965379delinsTGT	GRCh38
NC_000010.10:g.89725134_89725136delinsTGT , CM000672.1:g.89725134_89725136delinsTGT	GRCh37
NC_000010.9:g.89715114_89715116delinsTGT	NCBI36
NG_007466.2:g.106939_106941delinsTGT , LRG_311:g.106939_106941delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1210_1212delinsTGT	ENSP00000514759.2:p.Glu404Cys
ENST00000710265.1:c.*146_*148delinsTGT	ENSP00000518161.1:n.*146_*148delinsTGT
ENST00000688158.2:n.1852_1854delinsTGT
ENST00000688922.2:c.*947_*949delinsTGT	ENSP00000508742.2:n.*947_*949delinsTGT
ENST00000700021.1:c.1072_1074delinsTGT	ENSP00000514757.1:p.Glu358Cys
ENST00000700022.1:c.*456_*458delinsTGT	ENSP00000514758.1:n.*456_*458delinsTGT
ENST00000700023.1:n.2275_2277delinsTGT
ENST00000700024.1:n.2509_2511delinsTGT
ENST00000706954.1:c.1117_1119delinsTGT	ENSP00000516674.1:p.Glu373Cys
ENST00000706955.1:c.*1152_*1154delinsTGT	ENSP00000516675.1:n.*1152_*1154delinsTGT
ENST00000686459.1:c.*703_*705delinsTGT	ENSP00000508909.1:n.*703_*705delinsTGT
ENST00000688158.1:c.*1228_*1230delinsTGT	ENSP00000509254.1:n.*1228_*1230delinsTGT
ENST00000688308.1:c.1117_1119delinsTGT	ENSP00000508752.1:p.Glu373Cys
ENST00000688922.1:c.1038_1040delinsTGT
ENST00000693560.1:c.1636_1638delinsTGT	ENSP00000509861.1:p.Glu546Cys
ENST00000371953.8:c.1117_1119delinsTGT MANE Select	ENSP00000361021.3:p.Glu373Cys
ENST00000371953.7:c.1117_1119delinsTGT	ENSP00000361021.3:p.Glu373Cys
NM_000314.5:c.1117_1119delinsTGT	NP_000305.3:p.Glu373Cys
NM_000314.6:c.1117_1119delinsTGT	NP_000305.3:p.Glu373Cys
NM_001304717.2:c.1636_1638delinsTGT	NP_001291646.2:p.Glu546Cys
NM_001304718.1:c.526_528delinsTGT	NP_001291647.1:p.Glu176Cys
XM_006717926.2:c.1072_1074delinsTGT	XP_006717989.1:p.Glu358Cys
XM_011539982.1:c.1021_1023delinsTGT	XP_011538284.1:p.Glu341Cys
XR_945791.1:n.1687_1689delinsTGT
NM_000314.7:c.1117_1119delinsTGT	NP_000305.3:p.Glu373Cys
NM_001304717.5:c.1636_1638delinsTGT	NP_001291646.4:p.Glu546Cys
NM_001304718.2:c.526_528delinsTGT	NP_001291647.1:p.Glu176Cys
NM_000314.8:c.1117_1119delinsTGT MANE Select	NP_000305.3:p.Glu373Cys