Canonical Allele Identifier: CA891840788
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957948_87957949delinsAT , CM000672.2:g.87957948_87957949delinsAT GRCh38
NC_000010.10:g.89717705_89717706delinsAT , CM000672.1:g.89717705_89717706delinsAT GRCh37
NC_000010.9:g.89707685_89707686delinsAT NCBI36
NG_007466.2:g.99510_99511delinsAT , LRG_311:g.99510_99511delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.730_731delinsAT ENSP00000514759.2:p.Pro244Ile
ENST00000710265.1:c.730_731delinsAT ENSP00000518161.1:p.Pro244Ile
ENST00000472832.3:c.730_731delinsAT ENSP00000483066.2:p.Pro244Ile
ENST00000688158.2:n.1465_1466delinsAT
ENST00000688922.2:c.*560_*561delinsAT ENSP00000508742.2:n.*560_*561delinsAT
ENST00000700021.1:c.685_686delinsAT ENSP00000514757.1:p.Pro229Ile
ENST00000700022.1:c.*69_*70delinsAT ENSP00000514758.1:n.*69_*70delinsAT
ENST00000700023.1:n.1888_1889delinsAT
ENST00000700024.1:n.2122_2123delinsAT
ENST00000700025.1:n.1499_1500delinsAT
ENST00000700026.1:n.367_368delinsAT
ENST00000700029.1:c.564_565delinsAT
ENST00000706954.1:c.730_731delinsAT ENSP00000516674.1:p.Pro244Ile
ENST00000706955.1:c.*765_*766delinsAT ENSP00000516675.1:n.*765_*766delinsAT
ENST00000686459.1:c.*316_*317delinsAT ENSP00000508909.1:n.*316_*317delinsAT
ENST00000688158.1:c.*841_*842delinsAT ENSP00000509254.1:n.*841_*842delinsAT
ENST00000688308.1:c.730_731delinsAT ENSP00000508752.1:p.Pro244Ile
ENST00000688922.1:c.651_652delinsAT
ENST00000693560.1:c.1249_1250delinsAT ENSP00000509861.1:p.Pro417Ile
ENST00000371953.8:c.730_731delinsAT MANE Select ENSP00000361021.3:p.Pro244Ile
ENST00000371953.7:c.730_731delinsAT ENSP00000361021.3:p.Pro244Ile
ENST00000472832.2:c.157_158delinsAT ENSP00000483066.1:p.Pro53Ile
NM_000314.5:c.730_731delinsAT NP_000305.3:p.Pro244Ile
NM_000314.6:c.730_731delinsAT NP_000305.3:p.Pro244Ile
NM_001304717.2:c.1249_1250delinsAT NP_001291646.2:p.Pro417Ile
NM_001304718.1:c.139_140delinsAT NP_001291647.1:p.Pro47Ile
XM_006717926.2:c.685_686delinsAT XP_006717989.1:p.Pro229Ile
XM_011539981.1:c.730_731delinsAT XP_011538283.1:p.Pro244Ile
XM_011539982.1:c.634_635delinsAT XP_011538284.1:p.Pro212Ile
XR_945791.1:n.1300_1301delinsAT
NM_000314.7:c.730_731delinsAT NP_000305.3:p.Pro244Ile
NM_001304717.5:c.1249_1250delinsAT NP_001291646.4:p.Pro417Ile
NM_001304718.2:c.139_140delinsAT NP_001291647.1:p.Pro47Ile
NM_000314.8:c.730_731delinsAT MANE Select NP_000305.3:p.Pro244Ile