Canonical Allele Identifier: CA2579926612

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961099_87961100delinsCT , CM000672.2:g.87961099_87961100delinsCT	GRCh38
NC_000010.10:g.89720856_89720857delinsCT , CM000672.1:g.89720856_89720857delinsCT	GRCh37
NC_000010.9:g.89710836_89710837delinsCT	NCBI36
NG_007466.2:g.102661_102662delinsCT , LRG_311:g.102661_102662delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1100_1101delinsCT	ENSP00000514759.2:p.Tyr367Ser
ENST00000710265.1:c.1007_1008delinsCT	ENSP00000518161.1:p.Tyr336Ser
ENST00000472832.3:c.1007_1008delinsCT	ENSP00000483066.2:p.Tyr336Ser
ENST00000688158.2:n.1742_1743delinsCT
ENST00000688922.2:c.*837_*838delinsCT	ENSP00000508742.2:n.*837_*838delinsCT
ENST00000700021.1:c.962_963delinsCT	ENSP00000514757.1:p.Tyr321Ser
ENST00000700022.1:c.*346_*347delinsCT	ENSP00000514758.1:n.*346_*347delinsCT
ENST00000700023.1:n.2165_2166delinsCT
ENST00000700024.1:n.2399_2400delinsCT
ENST00000700025.1:n.1776_1777delinsCT
ENST00000700026.1:n.644_645delinsCT
ENST00000706954.1:c.1007_1008delinsCT	ENSP00000516674.1:p.Tyr336Ser
ENST00000706955.1:c.*1042_*1043delinsCT	ENSP00000516675.1:n.*1042_*1043delinsCT
ENST00000686459.1:c.*593_*594delinsCT	ENSP00000508909.1:n.*593_*594delinsCT
ENST00000688158.1:c.*1118_*1119delinsCT	ENSP00000509254.1:n.*1118_*1119delinsCT
ENST00000688308.1:c.1007_1008delinsCT	ENSP00000508752.1:p.Tyr336Ser
ENST00000688922.1:c.928_929delinsCT
ENST00000693560.1:c.1526_1527delinsCT	ENSP00000509861.1:p.Tyr509Ser
ENST00000371953.8:c.1007_1008delinsCT MANE Select	ENSP00000361021.3:p.Tyr336Ser
ENST00000371953.7:c.1007_1008delinsCT	ENSP00000361021.3:p.Tyr336Ser
ENST00000472832.2:c.434_435delinsCT	ENSP00000483066.1:p.Tyr145Ser
NM_000314.5:c.1007_1008delinsCT	NP_000305.3:p.Tyr336Ser
NM_000314.6:c.1007_1008delinsCT	NP_000305.3:p.Tyr336Ser
NM_001304717.2:c.1526_1527delinsCT	NP_001291646.2:p.Tyr509Ser
NM_001304718.1:c.416_417delinsCT	NP_001291647.1:p.Tyr139Ser
XM_006717926.2:c.962_963delinsCT	XP_006717989.1:p.Tyr321Ser
XM_011539981.1:c.1007_1008delinsCT	XP_011538283.1:p.Tyr336Ser
XM_011539982.1:c.911_912delinsCT	XP_011538284.1:p.Tyr304Ser
XR_945791.1:n.1577_1578delinsCT
NM_000314.7:c.1007_1008delinsCT	NP_000305.3:p.Tyr336Ser
NM_001304717.5:c.1526_1527delinsCT	NP_001291646.4:p.Tyr509Ser
NM_001304718.2:c.416_417delinsCT	NP_001291647.1:p.Tyr139Ser
NM_000314.8:c.1007_1008delinsCT MANE Select	NP_000305.3:p.Tyr336Ser