Canonical Allele Identifier: CA891840870
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957984_87957986delinsATT , CM000672.2:g.87957984_87957986delinsATT GRCh38
NC_000010.10:g.89717741_89717743delinsATT , CM000672.1:g.89717741_89717743delinsATT GRCh37
NC_000010.9:g.89707721_89707723delinsATT NCBI36
NG_007466.2:g.99546_99548delinsATT , LRG_311:g.99546_99548delinsATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.766_768delinsATT ENSP00000514759.2:p.Glu256Ile
ENST00000710265.1:c.766_768delinsATT ENSP00000518161.1:p.Glu256Ile
ENST00000472832.3:c.766_768delinsATT ENSP00000483066.2:p.Glu256Ile
ENST00000688158.2:n.1501_1503delinsATT
ENST00000688922.2:c.*596_*598delinsATT ENSP00000508742.2:n.*596_*598delinsATT
ENST00000700021.1:c.721_723delinsATT ENSP00000514757.1:p.Glu241Ile
ENST00000700022.1:c.*105_*107delinsATT ENSP00000514758.1:n.*105_*107delinsATT
ENST00000700023.1:n.1924_1926delinsATT
ENST00000700024.1:n.2158_2160delinsATT
ENST00000700025.1:n.1535_1537delinsATT
ENST00000700026.1:n.403_405delinsATT
ENST00000700029.1:c.600_602delinsATT
ENST00000706954.1:c.766_768delinsATT ENSP00000516674.1:p.Glu256Ile
ENST00000706955.1:c.*801_*803delinsATT ENSP00000516675.1:n.*801_*803delinsATT
ENST00000686459.1:c.*352_*354delinsATT ENSP00000508909.1:n.*352_*354delinsATT
ENST00000688158.1:c.*877_*879delinsATT ENSP00000509254.1:n.*877_*879delinsATT
ENST00000688308.1:c.766_768delinsATT ENSP00000508752.1:p.Glu256Ile
ENST00000688922.1:c.687_689delinsATT
ENST00000693560.1:c.1285_1287delinsATT ENSP00000509861.1:p.Glu429Ile
ENST00000371953.8:c.766_768delinsATT MANE Select ENSP00000361021.3:p.Glu256Ile
ENST00000371953.7:c.766_768delinsATT ENSP00000361021.3:p.Glu256Ile
ENST00000472832.2:c.193_195delinsATT ENSP00000483066.1:p.Glu65Ile
NM_000314.5:c.766_768delinsATT NP_000305.3:p.Glu256Ile
NM_000314.6:c.766_768delinsATT NP_000305.3:p.Glu256Ile
NM_001304717.2:c.1285_1287delinsATT NP_001291646.2:p.Glu429Ile
NM_001304718.1:c.175_177delinsATT NP_001291647.1:p.Glu59Ile
XM_006717926.2:c.721_723delinsATT XP_006717989.1:p.Glu241Ile
XM_011539981.1:c.766_768delinsATT XP_011538283.1:p.Glu256Ile
XM_011539982.1:c.670_672delinsATT XP_011538284.1:p.Glu224Ile
XR_945791.1:n.1336_1338delinsATT
NM_000314.7:c.766_768delinsATT NP_000305.3:p.Glu256Ile
NM_001304717.5:c.1285_1287delinsATT NP_001291646.4:p.Glu429Ile
NM_001304718.2:c.175_177delinsATT NP_001291647.1:p.Glu59Ile
NM_000314.8:c.766_768delinsATT MANE Select NP_000305.3:p.Glu256Ile