Canonical Allele Identifier: CA891841604

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965362_87965363delinsCT , CM000672.2:g.87965362_87965363delinsCT	GRCh38
NC_000010.10:g.89725119_89725120delinsCT , CM000672.1:g.89725119_89725120delinsCT	GRCh37
NC_000010.9:g.89715099_89715100delinsCT	NCBI36
NG_007466.2:g.106924_106925delinsCT , LRG_311:g.106924_106925delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1195_1196delinsCT	ENSP00000514759.2:p.Asp399Leu
ENST00000710265.1:c.*131_*132delinsCT	ENSP00000518161.1:n.*131_*132delinsCT
ENST00000688158.2:n.1837_1838delinsCT
ENST00000688922.2:c.*932_*933delinsCT	ENSP00000508742.2:n.*932_*933delinsCT
ENST00000700021.1:c.1057_1058delinsCT	ENSP00000514757.1:p.Asp353Leu
ENST00000700022.1:c.*441_*442delinsCT	ENSP00000514758.1:n.*441_*442delinsCT
ENST00000700023.1:n.2260_2261delinsCT
ENST00000700024.1:n.2494_2495delinsCT
ENST00000706954.1:c.1102_1103delinsCT	ENSP00000516674.1:p.Asp368Leu
ENST00000706955.1:c.*1137_*1138delinsCT	ENSP00000516675.1:n.*1137_*1138delinsCT
ENST00000686459.1:c.*688_*689delinsCT	ENSP00000508909.1:n.*688_*689delinsCT
ENST00000688158.1:c.*1213_*1214delinsCT	ENSP00000509254.1:n.*1213_*1214delinsCT
ENST00000688308.1:c.1102_1103delinsCT	ENSP00000508752.1:p.Asp368Leu
ENST00000688922.1:c.1023_1024delinsCT
ENST00000693560.1:c.1621_1622delinsCT	ENSP00000509861.1:p.Asp541Leu
ENST00000371953.8:c.1102_1103delinsCT MANE Select	ENSP00000361021.3:p.Asp368Leu
ENST00000371953.7:c.1102_1103delinsCT	ENSP00000361021.3:p.Asp368Leu
NM_000314.5:c.1102_1103delinsCT	NP_000305.3:p.Asp368Leu
NM_000314.6:c.1102_1103delinsCT	NP_000305.3:p.Asp368Leu
NM_001304717.2:c.1621_1622delinsCT	NP_001291646.2:p.Asp541Leu
NM_001304718.1:c.511_512delinsCT	NP_001291647.1:p.Asp171Leu
XM_006717926.2:c.1057_1058delinsCT	XP_006717989.1:p.Asp353Leu
XM_011539982.1:c.1006_1007delinsCT	XP_011538284.1:p.Asp336Leu
XR_945791.1:n.1672_1673delinsCT
NM_000314.7:c.1102_1103delinsCT	NP_000305.3:p.Asp368Leu
NM_001304717.5:c.1621_1622delinsCT	NP_001291646.4:p.Asp541Leu
NM_001304718.2:c.511_512delinsCT	NP_001291647.1:p.Asp171Leu
NM_000314.8:c.1102_1103delinsCT MANE Select	NP_000305.3:p.Asp368Leu