Canonical Allele Identifier: CA891837741
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965386_87965387delinsTT , CM000672.2:g.87965386_87965387delinsTT GRCh38
NC_000010.10:g.89725143_89725144delinsTT , CM000672.1:g.89725143_89725144delinsTT GRCh37
NC_000010.9:g.89715123_89715124delinsTT NCBI36
NG_007466.2:g.106948_106949delinsTT , LRG_311:g.106948_106949delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1219_1220delinsTT ENSP00000514759.2:p.His407Phe
ENST00000710265.1:c.*155_*156delinsTT ENSP00000518161.1:n.*155_*156delinsTT
ENST00000688158.2:n.1861_1862delinsTT
ENST00000688922.2:c.*956_*957delinsTT ENSP00000508742.2:n.*956_*957delinsTT
ENST00000700021.1:c.1081_1082delinsTT ENSP00000514757.1:p.His361Phe
ENST00000700022.1:c.*465_*466delinsTT ENSP00000514758.1:n.*465_*466delinsTT
ENST00000700023.1:n.2284_2285delinsTT
ENST00000700024.1:n.2518_2519delinsTT
ENST00000706954.1:c.1126_1127delinsTT ENSP00000516674.1:p.His376Phe
ENST00000706955.1:c.*1161_*1162delinsTT ENSP00000516675.1:n.*1161_*1162delinsTT
ENST00000686459.1:c.*712_*713delinsTT ENSP00000508909.1:n.*712_*713delinsTT
ENST00000688158.1:c.*1237_*1238delinsTT ENSP00000509254.1:n.*1237_*1238delinsTT
ENST00000688308.1:c.1126_1127delinsTT ENSP00000508752.1:p.His376Phe
ENST00000688922.1:c.1047_1048delinsTT
ENST00000693560.1:c.1645_1646delinsTT ENSP00000509861.1:p.His549Phe
ENST00000371953.8:c.1126_1127delinsTT MANE Select ENSP00000361021.3:p.His376Phe
ENST00000371953.7:c.1126_1127delinsTT ENSP00000361021.3:p.His376Phe
NM_000314.5:c.1126_1127delinsTT NP_000305.3:p.His376Phe
NM_000314.6:c.1126_1127delinsTT NP_000305.3:p.His376Phe
NM_001304717.2:c.1645_1646delinsTT NP_001291646.2:p.His549Phe
NM_001304718.1:c.535_536delinsTT NP_001291647.1:p.His179Phe
XM_006717926.2:c.1081_1082delinsTT XP_006717989.1:p.His361Phe
XM_011539982.1:c.1030_1031delinsTT XP_011538284.1:p.His344Phe
XR_945791.1:n.1696_1697delinsTT
NM_000314.7:c.1126_1127delinsTT NP_000305.3:p.His376Phe
NM_001304717.5:c.1645_1646delinsTT NP_001291646.4:p.His549Phe
NM_001304718.2:c.535_536delinsTT NP_001291647.1:p.His179Phe
NM_000314.8:c.1126_1127delinsTT MANE Select NP_000305.3:p.His376Phe