Canonical Allele Identifier: CA891837523
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965362_87965363delinsAC , CM000672.2:g.87965362_87965363delinsAC GRCh38
NC_000010.10:g.89725119_89725120delinsAC , CM000672.1:g.89725119_89725120delinsAC GRCh37
NC_000010.9:g.89715099_89715100delinsAC NCBI36
NG_007466.2:g.106924_106925delinsAC , LRG_311:g.106924_106925delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1195_1196delinsAC ENSP00000514759.2:p.Asp399Thr
ENST00000710265.1:c.*131_*132delinsAC ENSP00000518161.1:n.*131_*132delinsAC
ENST00000688158.2:n.1837_1838delinsAC
ENST00000688922.2:c.*932_*933delinsAC ENSP00000508742.2:n.*932_*933delinsAC
ENST00000700021.1:c.1057_1058delinsAC ENSP00000514757.1:p.Asp353Thr
ENST00000700022.1:c.*441_*442delinsAC ENSP00000514758.1:n.*441_*442delinsAC
ENST00000700023.1:n.2260_2261delinsAC
ENST00000700024.1:n.2494_2495delinsAC
ENST00000706954.1:c.1102_1103delinsAC ENSP00000516674.1:p.Asp368Thr
ENST00000706955.1:c.*1137_*1138delinsAC ENSP00000516675.1:n.*1137_*1138delinsAC
ENST00000686459.1:c.*688_*689delinsAC ENSP00000508909.1:n.*688_*689delinsAC
ENST00000688158.1:c.*1213_*1214delinsAC ENSP00000509254.1:n.*1213_*1214delinsAC
ENST00000688308.1:c.1102_1103delinsAC ENSP00000508752.1:p.Asp368Thr
ENST00000688922.1:c.1023_1024delinsAC
ENST00000693560.1:c.1621_1622delinsAC ENSP00000509861.1:p.Asp541Thr
ENST00000371953.8:c.1102_1103delinsAC MANE Select ENSP00000361021.3:p.Asp368Thr
ENST00000371953.7:c.1102_1103delinsAC ENSP00000361021.3:p.Asp368Thr
NM_000314.5:c.1102_1103delinsAC NP_000305.3:p.Asp368Thr
NM_000314.6:c.1102_1103delinsAC NP_000305.3:p.Asp368Thr
NM_001304717.2:c.1621_1622delinsAC NP_001291646.2:p.Asp541Thr
NM_001304718.1:c.511_512delinsAC NP_001291647.1:p.Asp171Thr
XM_006717926.2:c.1057_1058delinsAC XP_006717989.1:p.Asp353Thr
XM_011539982.1:c.1006_1007delinsAC XP_011538284.1:p.Asp336Thr
XR_945791.1:n.1672_1673delinsAC
NM_000314.7:c.1102_1103delinsAC NP_000305.3:p.Asp368Thr
NM_001304717.5:c.1621_1622delinsAC NP_001291646.4:p.Asp541Thr
NM_001304718.2:c.511_512delinsAC NP_001291647.1:p.Asp171Thr
NM_000314.8:c.1102_1103delinsAC MANE Select NP_000305.3:p.Asp368Thr