Canonical Allele Identifier: CA891837770
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965389_87965390delinsAC , CM000672.2:g.87965389_87965390delinsAC GRCh38
NC_000010.10:g.89725146_89725147delinsAC , CM000672.1:g.89725146_89725147delinsAC GRCh37
NC_000010.9:g.89715126_89715127delinsAC NCBI36
NG_007466.2:g.106951_106952delinsAC , LRG_311:g.106951_106952delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1222_1223delinsAC ENSP00000514759.2:p.Tyr408Thr
ENST00000710265.1:c.*158_*159delinsAC ENSP00000518161.1:n.*158_*159delinsAC
ENST00000688158.2:n.1864_1865delinsAC
ENST00000688922.2:c.*959_*960delinsAC ENSP00000508742.2:n.*959_*960delinsAC
ENST00000700021.1:c.1084_1085delinsAC ENSP00000514757.1:p.Tyr362Thr
ENST00000700022.1:c.*468_*469delinsAC ENSP00000514758.1:n.*468_*469delinsAC
ENST00000700023.1:n.2287_2288delinsAC
ENST00000700024.1:n.2521_2522delinsAC
ENST00000706954.1:c.1129_1130delinsAC ENSP00000516674.1:p.Tyr377Thr
ENST00000706955.1:c.*1164_*1165delinsAC ENSP00000516675.1:n.*1164_*1165delinsAC
ENST00000686459.1:c.*715_*716delinsAC ENSP00000508909.1:n.*715_*716delinsAC
ENST00000688158.1:c.*1240_*1241delinsAC ENSP00000509254.1:n.*1240_*1241delinsAC
ENST00000688308.1:c.1129_1130delinsAC ENSP00000508752.1:p.Tyr377Thr
ENST00000688922.1:c.1050_1051delinsAC
ENST00000693560.1:c.1648_1649delinsAC ENSP00000509861.1:p.Tyr550Thr
ENST00000371953.8:c.1129_1130delinsAC MANE Select ENSP00000361021.3:p.Tyr377Thr
ENST00000371953.7:c.1129_1130delinsAC ENSP00000361021.3:p.Tyr377Thr
NM_000314.5:c.1129_1130delinsAC NP_000305.3:p.Tyr377Thr
NM_000314.6:c.1129_1130delinsAC NP_000305.3:p.Tyr377Thr
NM_001304717.2:c.1648_1649delinsAC NP_001291646.2:p.Tyr550Thr
NM_001304718.1:c.538_539delinsAC NP_001291647.1:p.Tyr180Thr
XM_006717926.2:c.1084_1085delinsAC XP_006717989.1:p.Tyr362Thr
XM_011539982.1:c.1033_1034delinsAC XP_011538284.1:p.Tyr345Thr
XR_945791.1:n.1699_1700delinsAC
NM_000314.7:c.1129_1130delinsAC NP_000305.3:p.Tyr377Thr
NM_001304717.5:c.1648_1649delinsAC NP_001291646.4:p.Tyr550Thr
NM_001304718.2:c.538_539delinsAC NP_001291647.1:p.Tyr180Thr
NM_000314.8:c.1129_1130delinsAC MANE Select NP_000305.3:p.Tyr377Thr