Canonical Allele Identifier: CA891838141
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965443_87965444delinsTC , CM000672.2:g.87965443_87965444delinsTC GRCh38
NC_000010.10:g.89725200_89725201delinsTC , CM000672.1:g.89725200_89725201delinsTC GRCh37
NC_000010.9:g.89715180_89715181delinsTC NCBI36
NG_007466.2:g.107005_107006delinsTC , LRG_311:g.107005_107006delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1276_1277delinsTC ENSP00000514759.2:p.Asp426Ser
ENST00000710265.1:c.*212_*213delinsTC ENSP00000518161.1:n.*212_*213delinsTC
ENST00000688158.2:n.1918_1919delinsTC
ENST00000688922.2:c.*1013_*1014delinsTC ENSP00000508742.2:n.*1013_*1014delinsTC
ENST00000700021.1:c.1138_1139delinsTC ENSP00000514757.1:p.Asp380Ser
ENST00000700022.1:c.*522_*523delinsTC ENSP00000514758.1:n.*522_*523delinsTC
ENST00000700023.1:n.2341_2342delinsTC
ENST00000700024.1:n.2575_2576delinsTC
ENST00000706954.1:c.1183_1184delinsTC ENSP00000516674.1:p.Asp395Ser
ENST00000706955.1:c.*1218_*1219delinsTC ENSP00000516675.1:n.*1218_*1219delinsTC
ENST00000686459.1:c.*769_*770delinsTC ENSP00000508909.1:n.*769_*770delinsTC
ENST00000688158.1:c.*1294_*1295delinsTC ENSP00000509254.1:n.*1294_*1295delinsTC
ENST00000688308.1:c.1183_1184delinsTC ENSP00000508752.1:p.Asp395Ser
ENST00000688922.1:c.1104_1105delinsTC
ENST00000693560.1:c.1702_1703delinsTC ENSP00000509861.1:p.Asp568Ser
ENST00000371953.8:c.1183_1184delinsTC MANE Select ENSP00000361021.3:p.Asp395Ser
ENST00000371953.7:c.1183_1184delinsTC ENSP00000361021.3:p.Asp395Ser
NM_000314.5:c.1183_1184delinsTC NP_000305.3:p.Asp395Ser
NM_000314.6:c.1183_1184delinsTC NP_000305.3:p.Asp395Ser
NM_001304717.2:c.1702_1703delinsTC NP_001291646.2:p.Asp568Ser
NM_001304718.1:c.592_593delinsTC NP_001291647.1:p.Asp198Ser
XM_006717926.2:c.1138_1139delinsTC XP_006717989.1:p.Asp380Ser
XM_011539982.1:c.1087_1088delinsTC XP_011538284.1:p.Asp363Ser
XR_945791.1:n.1753_1754delinsTC
NM_000314.7:c.1183_1184delinsTC NP_000305.3:p.Asp395Ser
NM_001304717.5:c.1702_1703delinsTC NP_001291646.4:p.Asp568Ser
NM_001304718.2:c.592_593delinsTC NP_001291647.1:p.Asp198Ser
NM_000314.8:c.1183_1184delinsTC MANE Select NP_000305.3:p.Asp395Ser