Canonical Allele Identifier: CA891837716
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965383_87965385delinsATG , CM000672.2:g.87965383_87965385delinsATG GRCh38
NC_000010.10:g.89725140_89725142delinsATG , CM000672.1:g.89725140_89725142delinsATG GRCh37
NC_000010.9:g.89715120_89715122delinsATG NCBI36
NG_007466.2:g.106945_106947delinsATG , LRG_311:g.106945_106947delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1216_1218delinsATG ENSP00000514759.2:p.Asp406Met
ENST00000710265.1:c.*152_*154delinsATG ENSP00000518161.1:n.*152_*154delinsATG
ENST00000688158.2:n.1858_1860delinsATG
ENST00000688922.2:c.*953_*955delinsATG ENSP00000508742.2:n.*953_*955delinsATG
ENST00000700021.1:c.1078_1080delinsATG ENSP00000514757.1:p.Asp360Met
ENST00000700022.1:c.*462_*464delinsATG ENSP00000514758.1:n.*462_*464delinsATG
ENST00000700023.1:n.2281_2283delinsATG
ENST00000700024.1:n.2515_2517delinsATG
ENST00000706954.1:c.1123_1125delinsATG ENSP00000516674.1:p.Asp375Met
ENST00000706955.1:c.*1158_*1160delinsATG ENSP00000516675.1:n.*1158_*1160delinsATG
ENST00000686459.1:c.*709_*711delinsATG ENSP00000508909.1:n.*709_*711delinsATG
ENST00000688158.1:c.*1234_*1236delinsATG ENSP00000509254.1:n.*1234_*1236delinsATG
ENST00000688308.1:c.1123_1125delinsATG ENSP00000508752.1:p.Asp375Met
ENST00000688922.1:c.1044_1046delinsATG
ENST00000693560.1:c.1642_1644delinsATG ENSP00000509861.1:p.Asp548Met
ENST00000371953.8:c.1123_1125delinsATG MANE Select ENSP00000361021.3:p.Asp375Met
ENST00000371953.7:c.1123_1125delinsATG ENSP00000361021.3:p.Asp375Met
NM_000314.5:c.1123_1125delinsATG NP_000305.3:p.Asp375Met
NM_000314.6:c.1123_1125delinsATG NP_000305.3:p.Asp375Met
NM_001304717.2:c.1642_1644delinsATG NP_001291646.2:p.Asp548Met
NM_001304718.1:c.532_534delinsATG NP_001291647.1:p.Asp178Met
XM_006717926.2:c.1078_1080delinsATG XP_006717989.1:p.Asp360Met
XM_011539982.1:c.1027_1029delinsATG XP_011538284.1:p.Asp343Met
XR_945791.1:n.1693_1695delinsATG
NM_000314.7:c.1123_1125delinsATG NP_000305.3:p.Asp375Met
NM_001304717.5:c.1642_1644delinsATG NP_001291646.4:p.Asp548Met
NM_001304718.2:c.532_534delinsATG NP_001291647.1:p.Asp178Met
NM_000314.8:c.1123_1125delinsATG MANE Select NP_000305.3:p.Asp375Met