Canonical Allele Identifier: CA891836058

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961011_87961013delinsTGT , CM000672.2:g.87961011_87961013delinsTGT	GRCh38
NC_000010.10:g.89720768_89720770delinsTGT , CM000672.1:g.89720768_89720770delinsTGT	GRCh37
NC_000010.9:g.89710748_89710750delinsTGT	NCBI36
NG_007466.2:g.102573_102575delinsTGT , LRG_311:g.102573_102575delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1012_1014delinsTGT	ENSP00000514759.2:p.Glu338Cys
ENST00000710265.1:c.919_921delinsTGT	ENSP00000518161.1:p.Glu307Cys
ENST00000472832.3:c.919_921delinsTGT	ENSP00000483066.2:p.Glu307Cys
ENST00000688158.2:n.1654_1656delinsTGT
ENST00000688922.2:c.*749_*751delinsTGT	ENSP00000508742.2:n.*749_*751delinsTGT
ENST00000700021.1:c.874_876delinsTGT	ENSP00000514757.1:p.Glu292Cys
ENST00000700022.1:c.*258_*260delinsTGT	ENSP00000514758.1:n.*258_*260delinsTGT
ENST00000700023.1:n.2077_2079delinsTGT
ENST00000700024.1:n.2311_2313delinsTGT
ENST00000700025.1:n.1688_1690delinsTGT
ENST00000700026.1:n.556_558delinsTGT
ENST00000706954.1:c.919_921delinsTGT	ENSP00000516674.1:p.Glu307Cys
ENST00000706955.1:c.*954_*956delinsTGT	ENSP00000516675.1:n.*954_*956delinsTGT
ENST00000686459.1:c.*505_*507delinsTGT	ENSP00000508909.1:n.*505_*507delinsTGT
ENST00000688158.1:c.*1030_*1032delinsTGT	ENSP00000509254.1:n.*1030_*1032delinsTGT
ENST00000688308.1:c.919_921delinsTGT	ENSP00000508752.1:p.Glu307Cys
ENST00000688922.1:c.840_842delinsTGT
ENST00000693560.1:c.1438_1440delinsTGT	ENSP00000509861.1:p.Glu480Cys
ENST00000371953.8:c.919_921delinsTGT MANE Select	ENSP00000361021.3:p.Glu307Cys
ENST00000371953.7:c.919_921delinsTGT	ENSP00000361021.3:p.Glu307Cys
ENST00000472832.2:c.346_348delinsTGT	ENSP00000483066.1:p.Glu116Cys
NM_000314.5:c.919_921delinsTGT	NP_000305.3:p.Glu307Cys
NM_000314.6:c.919_921delinsTGT	NP_000305.3:p.Glu307Cys
NM_001304717.2:c.1438_1440delinsTGT	NP_001291646.2:p.Glu480Cys
NM_001304718.1:c.328_330delinsTGT	NP_001291647.1:p.Glu110Cys
XM_006717926.2:c.874_876delinsTGT	XP_006717989.1:p.Glu292Cys
XM_011539981.1:c.919_921delinsTGT	XP_011538283.1:p.Glu307Cys
XM_011539982.1:c.823_825delinsTGT	XP_011538284.1:p.Glu275Cys
XR_945791.1:n.1489_1491delinsTGT
NM_000314.7:c.919_921delinsTGT	NP_000305.3:p.Glu307Cys
NM_001304717.5:c.1438_1440delinsTGT	NP_001291646.4:p.Glu480Cys
NM_001304718.2:c.328_330delinsTGT	NP_001291647.1:p.Glu110Cys
NM_000314.8:c.919_921delinsTGT MANE Select	NP_000305.3:p.Glu307Cys