Canonical Allele Identifier: CA891837056
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965311_87965313delinsTTT , CM000672.2:g.87965311_87965313delinsTTT GRCh38
NC_000010.10:g.89725068_89725070delinsTTT , CM000672.1:g.89725068_89725070delinsTTT GRCh37
NC_000010.9:g.89715048_89715050delinsTTT NCBI36
NG_007466.2:g.106873_106875delinsTTT , LRG_311:g.106873_106875delinsTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1144_1146delinsTTT ENSP00000514759.2:p.Val382Phe
ENST00000710265.1:c.*80_*82delinsTTT ENSP00000518161.1:n.*80_*82delinsTTT
ENST00000688158.2:n.1786_1788delinsTTT
ENST00000688922.2:c.*881_*883delinsTTT ENSP00000508742.2:n.*881_*883delinsTTT
ENST00000700021.1:c.1006_1008delinsTTT ENSP00000514757.1:p.Val336Phe
ENST00000700022.1:c.*390_*392delinsTTT ENSP00000514758.1:n.*390_*392delinsTTT
ENST00000700023.1:n.2209_2211delinsTTT
ENST00000700024.1:n.2443_2445delinsTTT
ENST00000706954.1:c.1051_1053delinsTTT ENSP00000516674.1:p.Val351Phe
ENST00000706955.1:c.*1086_*1088delinsTTT ENSP00000516675.1:n.*1086_*1088delinsTTT
ENST00000686459.1:c.*637_*639delinsTTT ENSP00000508909.1:n.*637_*639delinsTTT
ENST00000688158.1:c.*1162_*1164delinsTTT ENSP00000509254.1:n.*1162_*1164delinsTTT
ENST00000688308.1:c.1051_1053delinsTTT ENSP00000508752.1:p.Val351Phe
ENST00000688922.1:c.972_974delinsTTT
ENST00000693560.1:c.1570_1572delinsTTT ENSP00000509861.1:p.Val524Phe
ENST00000371953.8:c.1051_1053delinsTTT MANE Select ENSP00000361021.3:p.Val351Phe
ENST00000371953.7:c.1051_1053delinsTTT ENSP00000361021.3:p.Val351Phe
NM_000314.5:c.1051_1053delinsTTT NP_000305.3:p.Val351Phe
NM_000314.6:c.1051_1053delinsTTT NP_000305.3:p.Val351Phe
NM_001304717.2:c.1570_1572delinsTTT NP_001291646.2:p.Val524Phe
NM_001304718.1:c.460_462delinsTTT NP_001291647.1:p.Val154Phe
XM_006717926.2:c.1006_1008delinsTTT XP_006717989.1:p.Val336Phe
XM_011539982.1:c.955_957delinsTTT XP_011538284.1:p.Val319Phe
XR_945791.1:n.1621_1623delinsTTT
NM_000314.7:c.1051_1053delinsTTT NP_000305.3:p.Val351Phe
NM_001304717.5:c.1570_1572delinsTTT NP_001291646.4:p.Val524Phe
NM_001304718.2:c.460_462delinsTTT NP_001291647.1:p.Val154Phe
NM_000314.8:c.1051_1053delinsTTT MANE Select NP_000305.3:p.Val351Phe