Canonical Allele Identifier: CA891841265

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952133_87952134delinsGC , CM000672.2:g.87952133_87952134delinsGC	GRCh38
NC_000010.10:g.89711890_89711891delinsGC , CM000672.1:g.89711890_89711891delinsGC	GRCh37
NC_000010.9:g.89701870_89701871delinsGC	NCBI36
NG_007466.2:g.93695_93696delinsGC , LRG_311:g.93695_93696delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.508_509delinsGC	ENSP00000514759.2:p.Ser170Ala
ENST00000710265.1:c.508_509delinsGC	ENSP00000518161.1:p.Ser170Ala
ENST00000472832.3:c.508_509delinsGC	ENSP00000483066.2:p.Ser170Ala
ENST00000688158.2:n.1243_1244delinsGC
ENST00000688922.2:c.*338_*339delinsGC	ENSP00000508742.2:n.*338_*339delinsGC
ENST00000700021.1:c.463_464delinsGC	ENSP00000514757.1:p.Ser155Ala
ENST00000700022.1:c.493-5720_493-5719delinsGC	ENSP00000514758.1:n.493-5720_493-5719delinsGC
ENST00000700023.1:n.1666_1667delinsGC
ENST00000700024.1:n.1900_1901delinsGC
ENST00000700025.1:n.1277_1278delinsGC
ENST00000700029.1:c.342_343delinsGC
ENST00000706954.1:c.508_509delinsGC	ENSP00000516674.1:p.Ser170Ala
ENST00000706955.1:c.*543_*544delinsGC	ENSP00000516675.1:n.*543_*544delinsGC
ENST00000686459.1:c.*94_*95delinsGC	ENSP00000508909.1:n.*94_*95delinsGC
ENST00000688158.1:c.*619_*620delinsGC	ENSP00000509254.1:n.*619_*620delinsGC
ENST00000688308.1:c.508_509delinsGC	ENSP00000508752.1:p.Ser170Ala
ENST00000688922.1:c.429_430delinsGC
ENST00000693560.1:c.1027_1028delinsGC	ENSP00000509861.1:p.Ser343Ala
ENST00000371953.8:c.508_509delinsGC MANE Select	ENSP00000361021.3:p.Ser170Ala
ENST00000371953.7:c.508_509delinsGC	ENSP00000361021.3:p.Ser170Ala
NM_000314.5:c.508_509delinsGC	NP_000305.3:p.Ser170Ala
NM_000314.6:c.508_509delinsGC	NP_000305.3:p.Ser170Ala
NM_001304717.2:c.1027_1028delinsGC	NP_001291646.2:p.Ser343Ala
NM_001304718.1:c.-84_-83delinsGC	NP_001291647.1:n.-84_-83delinsGC
XM_006717926.2:c.463_464delinsGC	XP_006717989.1:p.Ser155Ala
XM_011539981.1:c.508_509delinsGC	XP_011538283.1:p.Ser170Ala
XM_011539982.1:c.412_413delinsGC	XP_011538284.1:p.Ser138Ala
XR_945789.1:n.1379_1380delinsGC
XR_945790.1:n.1496_1497delinsGC
XR_945791.1:n.1205-5720_1205-5719delinsGC
NM_000314.7:c.508_509delinsGC	NP_000305.3:p.Ser170Ala
NM_001304717.5:c.1027_1028delinsGC	NP_001291646.4:p.Ser343Ala
NM_001304718.2:c.-84_-83delinsGC	NP_001291647.1:n.-84_-83delinsGC
NM_000314.8:c.508_509delinsGC MANE Select	NP_000305.3:p.Ser170Ala