Canonical Allele Identifier: CA891836091

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961012_87961013delinsTT , CM000672.2:g.87961012_87961013delinsTT	GRCh38
NC_000010.10:g.89720769_89720770delinsTT , CM000672.1:g.89720769_89720770delinsTT	GRCh37
NC_000010.9:g.89710749_89710750delinsTT	NCBI36
NG_007466.2:g.102574_102575delinsTT , LRG_311:g.102574_102575delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1013_1014delinsTT	ENSP00000514759.2:p.Glu338Val
ENST00000710265.1:c.920_921delinsTT	ENSP00000518161.1:p.Glu307Val
ENST00000472832.3:c.920_921delinsTT	ENSP00000483066.2:p.Glu307Val
ENST00000688158.2:n.1655_1656delinsTT
ENST00000688922.2:c.*750_*751delinsTT	ENSP00000508742.2:n.*750_*751delinsTT
ENST00000700021.1:c.875_876delinsTT	ENSP00000514757.1:p.Glu292Val
ENST00000700022.1:c.*259_*260delinsTT	ENSP00000514758.1:n.*259_*260delinsTT
ENST00000700023.1:n.2078_2079delinsTT
ENST00000700024.1:n.2312_2313delinsTT
ENST00000700025.1:n.1689_1690delinsTT
ENST00000700026.1:n.557_558delinsTT
ENST00000706954.1:c.920_921delinsTT	ENSP00000516674.1:p.Glu307Val
ENST00000706955.1:c.*955_*956delinsTT	ENSP00000516675.1:n.*955_*956delinsTT
ENST00000686459.1:c.*506_*507delinsTT	ENSP00000508909.1:n.*506_*507delinsTT
ENST00000688158.1:c.*1031_*1032delinsTT	ENSP00000509254.1:n.*1031_*1032delinsTT
ENST00000688308.1:c.920_921delinsTT	ENSP00000508752.1:p.Glu307Val
ENST00000688922.1:c.841_842delinsTT
ENST00000693560.1:c.1439_1440delinsTT	ENSP00000509861.1:p.Glu480Val
ENST00000371953.8:c.920_921delinsTT MANE Select	ENSP00000361021.3:p.Glu307Val
ENST00000371953.7:c.920_921delinsTT	ENSP00000361021.3:p.Glu307Val
ENST00000472832.2:c.347_348delinsTT	ENSP00000483066.1:p.Glu116Val
NM_000314.5:c.920_921delinsTT	NP_000305.3:p.Glu307Val
NM_000314.6:c.920_921delinsTT	NP_000305.3:p.Glu307Val
NM_001304717.2:c.1439_1440delinsTT	NP_001291646.2:p.Glu480Val
NM_001304718.1:c.329_330delinsTT	NP_001291647.1:p.Glu110Val
XM_006717926.2:c.875_876delinsTT	XP_006717989.1:p.Glu292Val
XM_011539981.1:c.920_921delinsTT	XP_011538283.1:p.Glu307Val
XM_011539982.1:c.824_825delinsTT	XP_011538284.1:p.Glu275Val
XR_945791.1:n.1490_1491delinsTT
NM_000314.7:c.920_921delinsTT	NP_000305.3:p.Glu307Val
NM_001304717.5:c.1439_1440delinsTT	NP_001291646.4:p.Glu480Val
NM_001304718.2:c.329_330delinsTT	NP_001291647.1:p.Glu110Val
NM_000314.8:c.920_921delinsTT MANE Select	NP_000305.3:p.Glu307Val