Canonical Allele Identifier: CA2579986010
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965434_87965435delinsAC , CM000672.2:g.87965434_87965435delinsAC GRCh38
NC_000010.10:g.89725191_89725192delinsAC , CM000672.1:g.89725191_89725192delinsAC GRCh37
NC_000010.9:g.89715171_89715172delinsAC NCBI36
NG_007466.2:g.106996_106997delinsAC , LRG_311:g.106996_106997delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1267_1268delinsAC ENSP00000514759.2:p.Phe423Thr
ENST00000710265.1:c.*203_*204delinsAC ENSP00000518161.1:n.*203_*204delinsAC
ENST00000688158.2:n.1909_1910delinsAC
ENST00000688922.2:c.*1004_*1005delinsAC ENSP00000508742.2:n.*1004_*1005delinsAC
ENST00000700021.1:c.1129_1130delinsAC ENSP00000514757.1:p.Phe377Thr
ENST00000700022.1:c.*513_*514delinsAC ENSP00000514758.1:n.*513_*514delinsAC
ENST00000700023.1:n.2332_2333delinsAC
ENST00000700024.1:n.2566_2567delinsAC
ENST00000706954.1:c.1174_1175delinsAC ENSP00000516674.1:p.Phe392Thr
ENST00000706955.1:c.*1209_*1210delinsAC ENSP00000516675.1:n.*1209_*1210delinsAC
ENST00000686459.1:c.*760_*761delinsAC ENSP00000508909.1:n.*760_*761delinsAC
ENST00000688158.1:c.*1285_*1286delinsAC ENSP00000509254.1:n.*1285_*1286delinsAC
ENST00000688308.1:c.1174_1175delinsAC ENSP00000508752.1:p.Phe392Thr
ENST00000688922.1:c.1095_1096delinsAC
ENST00000693560.1:c.1693_1694delinsAC ENSP00000509861.1:p.Phe565Thr
ENST00000371953.8:c.1174_1175delinsAC MANE Select ENSP00000361021.3:p.Phe392Thr
ENST00000371953.7:c.1174_1175delinsAC ENSP00000361021.3:p.Phe392Thr
NM_000314.5:c.1174_1175delinsAC NP_000305.3:p.Phe392Thr
NM_000314.6:c.1174_1175delinsAC NP_000305.3:p.Phe392Thr
NM_001304717.2:c.1693_1694delinsAC NP_001291646.2:p.Phe565Thr
NM_001304718.1:c.583_584delinsAC NP_001291647.1:p.Phe195Thr
XM_006717926.2:c.1129_1130delinsAC XP_006717989.1:p.Phe377Thr
XM_011539982.1:c.1078_1079delinsAC XP_011538284.1:p.Phe360Thr
XR_945791.1:n.1744_1745delinsAC
NM_000314.7:c.1174_1175delinsAC NP_000305.3:p.Phe392Thr
NM_001304717.5:c.1693_1694delinsAC NP_001291646.4:p.Phe565Thr
NM_001304718.2:c.583_584delinsAC NP_001291647.1:p.Phe195Thr
NM_000314.8:c.1174_1175delinsAC MANE Select NP_000305.3:p.Phe392Thr