Canonical Allele Identifier: CA891838679

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952133_87952134delinsGA , CM000672.2:g.87952133_87952134delinsGA	GRCh38
NC_000010.10:g.89711890_89711891delinsGA , CM000672.1:g.89711890_89711891delinsGA	GRCh37
NC_000010.9:g.89701870_89701871delinsGA	NCBI36
NG_007466.2:g.93695_93696delinsGA , LRG_311:g.93695_93696delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.508_509delinsGA	ENSP00000514759.2:p.Ser170Asp
ENST00000710265.1:c.508_509delinsGA	ENSP00000518161.1:p.Ser170Asp
ENST00000472832.3:c.508_509delinsGA	ENSP00000483066.2:p.Ser170Asp
ENST00000688158.2:n.1243_1244delinsGA
ENST00000688922.2:c.*338_*339delinsGA	ENSP00000508742.2:n.*338_*339delinsGA
ENST00000700021.1:c.463_464delinsGA	ENSP00000514757.1:p.Ser155Asp
ENST00000700022.1:c.493-5720_493-5719delinsGA	ENSP00000514758.1:n.493-5720_493-5719delinsGA
ENST00000700023.1:n.1666_1667delinsGA
ENST00000700024.1:n.1900_1901delinsGA
ENST00000700025.1:n.1277_1278delinsGA
ENST00000700029.1:c.342_343delinsGA
ENST00000706954.1:c.508_509delinsGA	ENSP00000516674.1:p.Ser170Asp
ENST00000706955.1:c.*543_*544delinsGA	ENSP00000516675.1:n.*543_*544delinsGA
ENST00000686459.1:c.*94_*95delinsGA	ENSP00000508909.1:n.*94_*95delinsGA
ENST00000688158.1:c.*619_*620delinsGA	ENSP00000509254.1:n.*619_*620delinsGA
ENST00000688308.1:c.508_509delinsGA	ENSP00000508752.1:p.Ser170Asp
ENST00000688922.1:c.429_430delinsGA
ENST00000693560.1:c.1027_1028delinsGA	ENSP00000509861.1:p.Ser343Asp
ENST00000371953.8:c.508_509delinsGA MANE Select	ENSP00000361021.3:p.Ser170Asp
ENST00000371953.7:c.508_509delinsGA	ENSP00000361021.3:p.Ser170Asp
NM_000314.5:c.508_509delinsGA	NP_000305.3:p.Ser170Asp
NM_000314.6:c.508_509delinsGA	NP_000305.3:p.Ser170Asp
NM_001304717.2:c.1027_1028delinsGA	NP_001291646.2:p.Ser343Asp
NM_001304718.1:c.-84_-83delinsGA	NP_001291647.1:n.-84_-83delinsGA
XM_006717926.2:c.463_464delinsGA	XP_006717989.1:p.Ser155Asp
XM_011539981.1:c.508_509delinsGA	XP_011538283.1:p.Ser170Asp
XM_011539982.1:c.412_413delinsGA	XP_011538284.1:p.Ser138Asp
XR_945789.1:n.1379_1380delinsGA
XR_945790.1:n.1496_1497delinsGA
XR_945791.1:n.1205-5720_1205-5719delinsGA
NM_000314.7:c.508_509delinsGA	NP_000305.3:p.Ser170Asp
NM_001304717.5:c.1027_1028delinsGA	NP_001291646.4:p.Ser343Asp
NM_001304718.2:c.-84_-83delinsGA	NP_001291647.1:n.-84_-83delinsGA
NM_000314.8:c.508_509delinsGA MANE Select	NP_000305.3:p.Ser170Asp