Canonical Allele Identifier: CA891837278

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965333_87965334delinsCT , CM000672.2:g.87965333_87965334delinsCT	GRCh38
NC_000010.10:g.89725090_89725091delinsCT , CM000672.1:g.89725090_89725091delinsCT	GRCh37
NC_000010.9:g.89715070_89715071delinsCT	NCBI36
NG_007466.2:g.106895_106896delinsCT , LRG_311:g.106895_106896delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1166_1167delinsCT	ENSP00000514759.2:p.Glu389Ala
ENST00000710265.1:c.*102_*103delinsCT	ENSP00000518161.1:n.*102_*103delinsCT
ENST00000688158.2:n.1808_1809delinsCT
ENST00000688922.2:c.*903_*904delinsCT	ENSP00000508742.2:n.*903_*904delinsCT
ENST00000700021.1:c.1028_1029delinsCT	ENSP00000514757.1:p.Glu343Ala
ENST00000700022.1:c.*412_*413delinsCT	ENSP00000514758.1:n.*412_*413delinsCT
ENST00000700023.1:n.2231_2232delinsCT
ENST00000700024.1:n.2465_2466delinsCT
ENST00000706954.1:c.1073_1074delinsCT	ENSP00000516674.1:p.Glu358Ala
ENST00000706955.1:c.*1108_*1109delinsCT	ENSP00000516675.1:n.*1108_*1109delinsCT
ENST00000686459.1:c.*659_*660delinsCT	ENSP00000508909.1:n.*659_*660delinsCT
ENST00000688158.1:c.*1184_*1185delinsCT	ENSP00000509254.1:n.*1184_*1185delinsCT
ENST00000688308.1:c.1073_1074delinsCT	ENSP00000508752.1:p.Glu358Ala
ENST00000688922.1:c.994_995delinsCT
ENST00000693560.1:c.1592_1593delinsCT	ENSP00000509861.1:p.Glu531Ala
ENST00000371953.8:c.1073_1074delinsCT MANE Select	ENSP00000361021.3:p.Glu358Ala
ENST00000371953.7:c.1073_1074delinsCT	ENSP00000361021.3:p.Glu358Ala
NM_000314.5:c.1073_1074delinsCT	NP_000305.3:p.Glu358Ala
NM_000314.6:c.1073_1074delinsCT	NP_000305.3:p.Glu358Ala
NM_001304717.2:c.1592_1593delinsCT	NP_001291646.2:p.Glu531Ala
NM_001304718.1:c.482_483delinsCT	NP_001291647.1:p.Glu161Ala
XM_006717926.2:c.1028_1029delinsCT	XP_006717989.1:p.Glu343Ala
XM_011539982.1:c.977_978delinsCT	XP_011538284.1:p.Glu326Ala
XR_945791.1:n.1643_1644delinsCT
NM_000314.7:c.1073_1074delinsCT	NP_000305.3:p.Glu358Ala
NM_001304717.5:c.1592_1593delinsCT	NP_001291646.4:p.Glu531Ala
NM_001304718.2:c.482_483delinsCT	NP_001291647.1:p.Glu161Ala
NM_000314.8:c.1073_1074delinsCT MANE Select	NP_000305.3:p.Glu358Ala