Canonical Allele Identifier: CA891841625
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965389_87965390delinsCG , CM000672.2:g.87965389_87965390delinsCG GRCh38
NC_000010.10:g.89725146_89725147delinsCG , CM000672.1:g.89725146_89725147delinsCG GRCh37
NC_000010.9:g.89715126_89715127delinsCG NCBI36
NG_007466.2:g.106951_106952delinsCG , LRG_311:g.106951_106952delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1222_1223delinsCG ENSP00000514759.2:p.Tyr408Arg
ENST00000710265.1:c.*158_*159delinsCG ENSP00000518161.1:n.*158_*159delinsCG
ENST00000688158.2:n.1864_1865delinsCG
ENST00000688922.2:c.*959_*960delinsCG ENSP00000508742.2:n.*959_*960delinsCG
ENST00000700021.1:c.1084_1085delinsCG ENSP00000514757.1:p.Tyr362Arg
ENST00000700022.1:c.*468_*469delinsCG ENSP00000514758.1:n.*468_*469delinsCG
ENST00000700023.1:n.2287_2288delinsCG
ENST00000700024.1:n.2521_2522delinsCG
ENST00000706954.1:c.1129_1130delinsCG ENSP00000516674.1:p.Tyr377Arg
ENST00000706955.1:c.*1164_*1165delinsCG ENSP00000516675.1:n.*1164_*1165delinsCG
ENST00000686459.1:c.*715_*716delinsCG ENSP00000508909.1:n.*715_*716delinsCG
ENST00000688158.1:c.*1240_*1241delinsCG ENSP00000509254.1:n.*1240_*1241delinsCG
ENST00000688308.1:c.1129_1130delinsCG ENSP00000508752.1:p.Tyr377Arg
ENST00000688922.1:c.1050_1051delinsCG
ENST00000693560.1:c.1648_1649delinsCG ENSP00000509861.1:p.Tyr550Arg
ENST00000371953.8:c.1129_1130delinsCG MANE Select ENSP00000361021.3:p.Tyr377Arg
ENST00000371953.7:c.1129_1130delinsCG ENSP00000361021.3:p.Tyr377Arg
NM_000314.5:c.1129_1130delinsCG NP_000305.3:p.Tyr377Arg
NM_000314.6:c.1129_1130delinsCG NP_000305.3:p.Tyr377Arg
NM_001304717.2:c.1648_1649delinsCG NP_001291646.2:p.Tyr550Arg
NM_001304718.1:c.538_539delinsCG NP_001291647.1:p.Tyr180Arg
XM_006717926.2:c.1084_1085delinsCG XP_006717989.1:p.Tyr362Arg
XM_011539982.1:c.1033_1034delinsCG XP_011538284.1:p.Tyr345Arg
XR_945791.1:n.1699_1700delinsCG
NM_000314.7:c.1129_1130delinsCG NP_000305.3:p.Tyr377Arg
NM_001304717.5:c.1648_1649delinsCG NP_001291646.4:p.Tyr550Arg
NM_001304718.2:c.538_539delinsCG NP_001291647.1:p.Tyr180Arg
NM_000314.8:c.1129_1130delinsCG MANE Select NP_000305.3:p.Tyr377Arg