Canonical Allele Identifier: CA891837635
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965374_87965376delinsTTG , CM000672.2:g.87965374_87965376delinsTTG GRCh38
NC_000010.10:g.89725131_89725133delinsTTG , CM000672.1:g.89725131_89725133delinsTTG GRCh37
NC_000010.9:g.89715111_89715113delinsTTG NCBI36
NG_007466.2:g.106936_106938delinsTTG , LRG_311:g.106936_106938delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1207_1209delinsTTG ENSP00000514759.2:p.Asn403Leu
ENST00000710265.1:c.*143_*145delinsTTG ENSP00000518161.1:n.*143_*145delinsTTG
ENST00000688158.2:n.1849_1851delinsTTG
ENST00000688922.2:c.*944_*946delinsTTG ENSP00000508742.2:n.*944_*946delinsTTG
ENST00000700021.1:c.1069_1071delinsTTG ENSP00000514757.1:p.Asn357Leu
ENST00000700022.1:c.*453_*455delinsTTG ENSP00000514758.1:n.*453_*455delinsTTG
ENST00000700023.1:n.2272_2274delinsTTG
ENST00000700024.1:n.2506_2508delinsTTG
ENST00000706954.1:c.1114_1116delinsTTG ENSP00000516674.1:p.Asn372Leu
ENST00000706955.1:c.*1149_*1151delinsTTG ENSP00000516675.1:n.*1149_*1151delinsTTG
ENST00000686459.1:c.*700_*702delinsTTG ENSP00000508909.1:n.*700_*702delinsTTG
ENST00000688158.1:c.*1225_*1227delinsTTG ENSP00000509254.1:n.*1225_*1227delinsTTG
ENST00000688308.1:c.1114_1116delinsTTG ENSP00000508752.1:p.Asn372Leu
ENST00000688922.1:c.1035_1037delinsTTG
ENST00000693560.1:c.1633_1635delinsTTG ENSP00000509861.1:p.Asn545Leu
ENST00000371953.8:c.1114_1116delinsTTG MANE Select ENSP00000361021.3:p.Asn372Leu
ENST00000371953.7:c.1114_1116delinsTTG ENSP00000361021.3:p.Asn372Leu
NM_000314.5:c.1114_1116delinsTTG NP_000305.3:p.Asn372Leu
NM_000314.6:c.1114_1116delinsTTG NP_000305.3:p.Asn372Leu
NM_001304717.2:c.1633_1635delinsTTG NP_001291646.2:p.Asn545Leu
NM_001304718.1:c.523_525delinsTTG NP_001291647.1:p.Asn175Leu
XM_006717926.2:c.1069_1071delinsTTG XP_006717989.1:p.Asn357Leu
XM_011539982.1:c.1018_1020delinsTTG XP_011538284.1:p.Asn340Leu
XR_945791.1:n.1684_1686delinsTTG
NM_000314.7:c.1114_1116delinsTTG NP_000305.3:p.Asn372Leu
NM_001304717.5:c.1633_1635delinsTTG NP_001291646.4:p.Asn545Leu
NM_001304718.2:c.523_525delinsTTG NP_001291647.1:p.Asn175Leu
NM_000314.8:c.1114_1116delinsTTG MANE Select NP_000305.3:p.Asn372Leu