Canonical Allele Identifier: CA891836066

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961011_87961013delinsTAT , CM000672.2:g.87961011_87961013delinsTAT	GRCh38
NC_000010.10:g.89720768_89720770delinsTAT , CM000672.1:g.89720768_89720770delinsTAT	GRCh37
NC_000010.9:g.89710748_89710750delinsTAT	NCBI36
NG_007466.2:g.102573_102575delinsTAT , LRG_311:g.102573_102575delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1012_1014delinsTAT	ENSP00000514759.2:p.Glu338Tyr
ENST00000710265.1:c.919_921delinsTAT	ENSP00000518161.1:p.Glu307Tyr
ENST00000472832.3:c.919_921delinsTAT	ENSP00000483066.2:p.Glu307Tyr
ENST00000688158.2:n.1654_1656delinsTAT
ENST00000688922.2:c.*749_*751delinsTAT	ENSP00000508742.2:n.*749_*751delinsTAT
ENST00000700021.1:c.874_876delinsTAT	ENSP00000514757.1:p.Glu292Tyr
ENST00000700022.1:c.*258_*260delinsTAT	ENSP00000514758.1:n.*258_*260delinsTAT
ENST00000700023.1:n.2077_2079delinsTAT
ENST00000700024.1:n.2311_2313delinsTAT
ENST00000700025.1:n.1688_1690delinsTAT
ENST00000700026.1:n.556_558delinsTAT
ENST00000706954.1:c.919_921delinsTAT	ENSP00000516674.1:p.Glu307Tyr
ENST00000706955.1:c.*954_*956delinsTAT	ENSP00000516675.1:n.*954_*956delinsTAT
ENST00000686459.1:c.*505_*507delinsTAT	ENSP00000508909.1:n.*505_*507delinsTAT
ENST00000688158.1:c.*1030_*1032delinsTAT	ENSP00000509254.1:n.*1030_*1032delinsTAT
ENST00000688308.1:c.919_921delinsTAT	ENSP00000508752.1:p.Glu307Tyr
ENST00000688922.1:c.840_842delinsTAT
ENST00000693560.1:c.1438_1440delinsTAT	ENSP00000509861.1:p.Glu480Tyr
ENST00000371953.8:c.919_921delinsTAT MANE Select	ENSP00000361021.3:p.Glu307Tyr
ENST00000371953.7:c.919_921delinsTAT	ENSP00000361021.3:p.Glu307Tyr
ENST00000472832.2:c.346_348delinsTAT	ENSP00000483066.1:p.Glu116Tyr
NM_000314.5:c.919_921delinsTAT	NP_000305.3:p.Glu307Tyr
NM_000314.6:c.919_921delinsTAT	NP_000305.3:p.Glu307Tyr
NM_001304717.2:c.1438_1440delinsTAT	NP_001291646.2:p.Glu480Tyr
NM_001304718.1:c.328_330delinsTAT	NP_001291647.1:p.Glu110Tyr
XM_006717926.2:c.874_876delinsTAT	XP_006717989.1:p.Glu292Tyr
XM_011539981.1:c.919_921delinsTAT	XP_011538283.1:p.Glu307Tyr
XM_011539982.1:c.823_825delinsTAT	XP_011538284.1:p.Glu275Tyr
XR_945791.1:n.1489_1491delinsTAT
NM_000314.7:c.919_921delinsTAT	NP_000305.3:p.Glu307Tyr
NM_001304717.5:c.1438_1440delinsTAT	NP_001291646.4:p.Glu480Tyr
NM_001304718.2:c.328_330delinsTAT	NP_001291647.1:p.Glu110Tyr
NM_000314.8:c.919_921delinsTAT MANE Select	NP_000305.3:p.Glu307Tyr