Canonical Allele Identifier: CA891839789
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957948_87957949delinsGT , CM000672.2:g.87957948_87957949delinsGT GRCh38
NC_000010.10:g.89717705_89717706delinsGT , CM000672.1:g.89717705_89717706delinsGT GRCh37
NC_000010.9:g.89707685_89707686delinsGT NCBI36
NG_007466.2:g.99510_99511delinsGT , LRG_311:g.99510_99511delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.730_731delinsGT ENSP00000514759.2:p.Pro244Val
ENST00000710265.1:c.730_731delinsGT ENSP00000518161.1:p.Pro244Val
ENST00000472832.3:c.730_731delinsGT ENSP00000483066.2:p.Pro244Val
ENST00000688158.2:n.1465_1466delinsGT
ENST00000688922.2:c.*560_*561delinsGT ENSP00000508742.2:n.*560_*561delinsGT
ENST00000700021.1:c.685_686delinsGT ENSP00000514757.1:p.Pro229Val
ENST00000700022.1:c.*69_*70delinsGT ENSP00000514758.1:n.*69_*70delinsGT
ENST00000700023.1:n.1888_1889delinsGT
ENST00000700024.1:n.2122_2123delinsGT
ENST00000700025.1:n.1499_1500delinsGT
ENST00000700026.1:n.367_368delinsGT
ENST00000700029.1:c.564_565delinsGT
ENST00000706954.1:c.730_731delinsGT ENSP00000516674.1:p.Pro244Val
ENST00000706955.1:c.*765_*766delinsGT ENSP00000516675.1:n.*765_*766delinsGT
ENST00000686459.1:c.*316_*317delinsGT ENSP00000508909.1:n.*316_*317delinsGT
ENST00000688158.1:c.*841_*842delinsGT ENSP00000509254.1:n.*841_*842delinsGT
ENST00000688308.1:c.730_731delinsGT ENSP00000508752.1:p.Pro244Val
ENST00000688922.1:c.651_652delinsGT
ENST00000693560.1:c.1249_1250delinsGT ENSP00000509861.1:p.Pro417Val
ENST00000371953.8:c.730_731delinsGT MANE Select ENSP00000361021.3:p.Pro244Val
ENST00000371953.7:c.730_731delinsGT ENSP00000361021.3:p.Pro244Val
ENST00000472832.2:c.157_158delinsGT ENSP00000483066.1:p.Pro53Val
NM_000314.5:c.730_731delinsGT NP_000305.3:p.Pro244Val
NM_000314.6:c.730_731delinsGT NP_000305.3:p.Pro244Val
NM_001304717.2:c.1249_1250delinsGT NP_001291646.2:p.Pro417Val
NM_001304718.1:c.139_140delinsGT NP_001291647.1:p.Pro47Val
XM_006717926.2:c.685_686delinsGT XP_006717989.1:p.Pro229Val
XM_011539981.1:c.730_731delinsGT XP_011538283.1:p.Pro244Val
XM_011539982.1:c.634_635delinsGT XP_011538284.1:p.Pro212Val
XR_945791.1:n.1300_1301delinsGT
NM_000314.7:c.730_731delinsGT NP_000305.3:p.Pro244Val
NM_001304717.5:c.1249_1250delinsGT NP_001291646.4:p.Pro417Val
NM_001304718.2:c.139_140delinsGT NP_001291647.1:p.Pro47Val
NM_000314.8:c.730_731delinsGT MANE Select NP_000305.3:p.Pro244Val