Canonical Allele Identifier: CA891837636
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965374_87965375delinsTT , CM000672.2:g.87965374_87965375delinsTT GRCh38
NC_000010.10:g.89725131_89725132delinsTT , CM000672.1:g.89725131_89725132delinsTT GRCh37
NC_000010.9:g.89715111_89715112delinsTT NCBI36
NG_007466.2:g.106936_106937delinsTT , LRG_311:g.106936_106937delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1207_1208delinsTT ENSP00000514759.2:p.Asn403Phe
ENST00000710265.1:c.*143_*144delinsTT ENSP00000518161.1:n.*143_*144delinsTT
ENST00000688158.2:n.1849_1850delinsTT
ENST00000688922.2:c.*944_*945delinsTT ENSP00000508742.2:n.*944_*945delinsTT
ENST00000700021.1:c.1069_1070delinsTT ENSP00000514757.1:p.Asn357Phe
ENST00000700022.1:c.*453_*454delinsTT ENSP00000514758.1:n.*453_*454delinsTT
ENST00000700023.1:n.2272_2273delinsTT
ENST00000700024.1:n.2506_2507delinsTT
ENST00000706954.1:c.1114_1115delinsTT ENSP00000516674.1:p.Asn372Phe
ENST00000706955.1:c.*1149_*1150delinsTT ENSP00000516675.1:n.*1149_*1150delinsTT
ENST00000686459.1:c.*700_*701delinsTT ENSP00000508909.1:n.*700_*701delinsTT
ENST00000688158.1:c.*1225_*1226delinsTT ENSP00000509254.1:n.*1225_*1226delinsTT
ENST00000688308.1:c.1114_1115delinsTT ENSP00000508752.1:p.Asn372Phe
ENST00000688922.1:c.1035_1036delinsTT
ENST00000693560.1:c.1633_1634delinsTT ENSP00000509861.1:p.Asn545Phe
ENST00000371953.8:c.1114_1115delinsTT MANE Select ENSP00000361021.3:p.Asn372Phe
ENST00000371953.7:c.1114_1115delinsTT ENSP00000361021.3:p.Asn372Phe
NM_000314.5:c.1114_1115delinsTT NP_000305.3:p.Asn372Phe
NM_000314.6:c.1114_1115delinsTT NP_000305.3:p.Asn372Phe
NM_001304717.2:c.1633_1634delinsTT NP_001291646.2:p.Asn545Phe
NM_001304718.1:c.523_524delinsTT NP_001291647.1:p.Asn175Phe
XM_006717926.2:c.1069_1070delinsTT XP_006717989.1:p.Asn357Phe
XM_011539982.1:c.1018_1019delinsTT XP_011538284.1:p.Asn340Phe
XR_945791.1:n.1684_1685delinsTT
NM_000314.7:c.1114_1115delinsTT NP_000305.3:p.Asn372Phe
NM_001304717.5:c.1633_1634delinsTT NP_001291646.4:p.Asn545Phe
NM_001304718.2:c.523_524delinsTT NP_001291647.1:p.Asn175Phe
NM_000314.8:c.1114_1115delinsTT MANE Select NP_000305.3:p.Asn372Phe