Canonical Allele Identifier: CA891841690
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965443_87965444delinsAT , CM000672.2:g.87965443_87965444delinsAT GRCh38
NC_000010.10:g.89725200_89725201delinsAT , CM000672.1:g.89725200_89725201delinsAT GRCh37
NC_000010.9:g.89715180_89715181delinsAT NCBI36
NG_007466.2:g.107005_107006delinsAT , LRG_311:g.107005_107006delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1276_1277delinsAT ENSP00000514759.2:p.Asp426Ile
ENST00000710265.1:c.*212_*213delinsAT ENSP00000518161.1:n.*212_*213delinsAT
ENST00000688158.2:n.1918_1919delinsAT
ENST00000688922.2:c.*1013_*1014delinsAT ENSP00000508742.2:n.*1013_*1014delinsAT
ENST00000700021.1:c.1138_1139delinsAT ENSP00000514757.1:p.Asp380Ile
ENST00000700022.1:c.*522_*523delinsAT ENSP00000514758.1:n.*522_*523delinsAT
ENST00000700023.1:n.2341_2342delinsAT
ENST00000700024.1:n.2575_2576delinsAT
ENST00000706954.1:c.1183_1184delinsAT ENSP00000516674.1:p.Asp395Ile
ENST00000706955.1:c.*1218_*1219delinsAT ENSP00000516675.1:n.*1218_*1219delinsAT
ENST00000686459.1:c.*769_*770delinsAT ENSP00000508909.1:n.*769_*770delinsAT
ENST00000688158.1:c.*1294_*1295delinsAT ENSP00000509254.1:n.*1294_*1295delinsAT
ENST00000688308.1:c.1183_1184delinsAT ENSP00000508752.1:p.Asp395Ile
ENST00000688922.1:c.1104_1105delinsAT
ENST00000693560.1:c.1702_1703delinsAT ENSP00000509861.1:p.Asp568Ile
ENST00000371953.8:c.1183_1184delinsAT MANE Select ENSP00000361021.3:p.Asp395Ile
ENST00000371953.7:c.1183_1184delinsAT ENSP00000361021.3:p.Asp395Ile
NM_000314.5:c.1183_1184delinsAT NP_000305.3:p.Asp395Ile
NM_000314.6:c.1183_1184delinsAT NP_000305.3:p.Asp395Ile
NM_001304717.2:c.1702_1703delinsAT NP_001291646.2:p.Asp568Ile
NM_001304718.1:c.592_593delinsAT NP_001291647.1:p.Asp198Ile
XM_006717926.2:c.1138_1139delinsAT XP_006717989.1:p.Asp380Ile
XM_011539982.1:c.1087_1088delinsAT XP_011538284.1:p.Asp363Ile
XR_945791.1:n.1753_1754delinsAT
NM_000314.7:c.1183_1184delinsAT NP_000305.3:p.Asp395Ile
NM_001304717.5:c.1702_1703delinsAT NP_001291646.4:p.Asp568Ile
NM_001304718.2:c.592_593delinsAT NP_001291647.1:p.Asp198Ile
NM_000314.8:c.1183_1184delinsAT MANE Select NP_000305.3:p.Asp395Ile