Canonical Allele Identifier: CA891838686

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952133_87952134delinsTT , CM000672.2:g.87952133_87952134delinsTT	GRCh38
NC_000010.10:g.89711890_89711891delinsTT , CM000672.1:g.89711890_89711891delinsTT	GRCh37
NC_000010.9:g.89701870_89701871delinsTT	NCBI36
NG_007466.2:g.93695_93696delinsTT , LRG_311:g.93695_93696delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.508_509delinsTT	ENSP00000514759.2:p.Ser170Phe
ENST00000710265.1:c.508_509delinsTT	ENSP00000518161.1:p.Ser170Phe
ENST00000472832.3:c.508_509delinsTT	ENSP00000483066.2:p.Ser170Phe
ENST00000688158.2:n.1243_1244delinsTT
ENST00000688922.2:c.*338_*339delinsTT	ENSP00000508742.2:n.*338_*339delinsTT
ENST00000700021.1:c.463_464delinsTT	ENSP00000514757.1:p.Ser155Phe
ENST00000700022.1:c.493-5720_493-5719delinsTT	ENSP00000514758.1:n.493-5720_493-5719delinsTT
ENST00000700023.1:n.1666_1667delinsTT
ENST00000700024.1:n.1900_1901delinsTT
ENST00000700025.1:n.1277_1278delinsTT
ENST00000700029.1:c.342_343delinsTT
ENST00000706954.1:c.508_509delinsTT	ENSP00000516674.1:p.Ser170Phe
ENST00000706955.1:c.*543_*544delinsTT	ENSP00000516675.1:n.*543_*544delinsTT
ENST00000686459.1:c.*94_*95delinsTT	ENSP00000508909.1:n.*94_*95delinsTT
ENST00000688158.1:c.*619_*620delinsTT	ENSP00000509254.1:n.*619_*620delinsTT
ENST00000688308.1:c.508_509delinsTT	ENSP00000508752.1:p.Ser170Phe
ENST00000688922.1:c.429_430delinsTT
ENST00000693560.1:c.1027_1028delinsTT	ENSP00000509861.1:p.Ser343Phe
ENST00000371953.8:c.508_509delinsTT MANE Select	ENSP00000361021.3:p.Ser170Phe
ENST00000371953.7:c.508_509delinsTT	ENSP00000361021.3:p.Ser170Phe
NM_000314.5:c.508_509delinsTT	NP_000305.3:p.Ser170Phe
NM_000314.6:c.508_509delinsTT	NP_000305.3:p.Ser170Phe
NM_001304717.2:c.1027_1028delinsTT	NP_001291646.2:p.Ser343Phe
NM_001304718.1:c.-84_-83delinsTT	NP_001291647.1:n.-84_-83delinsTT
XM_006717926.2:c.463_464delinsTT	XP_006717989.1:p.Ser155Phe
XM_011539981.1:c.508_509delinsTT	XP_011538283.1:p.Ser170Phe
XM_011539982.1:c.412_413delinsTT	XP_011538284.1:p.Ser138Phe
XR_945789.1:n.1379_1380delinsTT
XR_945790.1:n.1496_1497delinsTT
XR_945791.1:n.1205-5720_1205-5719delinsTT
NM_000314.7:c.508_509delinsTT	NP_000305.3:p.Ser170Phe
NM_001304717.5:c.1027_1028delinsTT	NP_001291646.4:p.Ser343Phe
NM_001304718.2:c.-84_-83delinsTT	NP_001291647.1:n.-84_-83delinsTT
NM_000314.8:c.508_509delinsTT MANE Select	NP_000305.3:p.Ser170Phe