Canonical Allele Identifier: CA891841620
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965374_87965375delinsCT , CM000672.2:g.87965374_87965375delinsCT GRCh38
NC_000010.10:g.89725131_89725132delinsCT , CM000672.1:g.89725131_89725132delinsCT GRCh37
NC_000010.9:g.89715111_89715112delinsCT NCBI36
NG_007466.2:g.106936_106937delinsCT , LRG_311:g.106936_106937delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1207_1208delinsCT ENSP00000514759.2:p.Asn403Leu
ENST00000710265.1:c.*143_*144delinsCT ENSP00000518161.1:n.*143_*144delinsCT
ENST00000688158.2:n.1849_1850delinsCT
ENST00000688922.2:c.*944_*945delinsCT ENSP00000508742.2:n.*944_*945delinsCT
ENST00000700021.1:c.1069_1070delinsCT ENSP00000514757.1:p.Asn357Leu
ENST00000700022.1:c.*453_*454delinsCT ENSP00000514758.1:n.*453_*454delinsCT
ENST00000700023.1:n.2272_2273delinsCT
ENST00000700024.1:n.2506_2507delinsCT
ENST00000706954.1:c.1114_1115delinsCT ENSP00000516674.1:p.Asn372Leu
ENST00000706955.1:c.*1149_*1150delinsCT ENSP00000516675.1:n.*1149_*1150delinsCT
ENST00000686459.1:c.*700_*701delinsCT ENSP00000508909.1:n.*700_*701delinsCT
ENST00000688158.1:c.*1225_*1226delinsCT ENSP00000509254.1:n.*1225_*1226delinsCT
ENST00000688308.1:c.1114_1115delinsCT ENSP00000508752.1:p.Asn372Leu
ENST00000688922.1:c.1035_1036delinsCT
ENST00000693560.1:c.1633_1634delinsCT ENSP00000509861.1:p.Asn545Leu
ENST00000371953.8:c.1114_1115delinsCT MANE Select ENSP00000361021.3:p.Asn372Leu
ENST00000371953.7:c.1114_1115delinsCT ENSP00000361021.3:p.Asn372Leu
NM_000314.5:c.1114_1115delinsCT NP_000305.3:p.Asn372Leu
NM_000314.6:c.1114_1115delinsCT NP_000305.3:p.Asn372Leu
NM_001304717.2:c.1633_1634delinsCT NP_001291646.2:p.Asn545Leu
NM_001304718.1:c.523_524delinsCT NP_001291647.1:p.Asn175Leu
XM_006717926.2:c.1069_1070delinsCT XP_006717989.1:p.Asn357Leu
XM_011539982.1:c.1018_1019delinsCT XP_011538284.1:p.Asn340Leu
XR_945791.1:n.1684_1685delinsCT
NM_000314.7:c.1114_1115delinsCT NP_000305.3:p.Asn372Leu
NM_001304717.5:c.1633_1634delinsCT NP_001291646.4:p.Asn545Leu
NM_001304718.2:c.523_524delinsCT NP_001291647.1:p.Asn175Leu
NM_000314.8:c.1114_1115delinsCT MANE Select NP_000305.3:p.Asn372Leu