Canonical Allele Identifier: CA2579926782
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957984_87957986delinsACT , CM000672.2:g.87957984_87957986delinsACT GRCh38
NC_000010.10:g.89717741_89717743delinsACT , CM000672.1:g.89717741_89717743delinsACT GRCh37
NC_000010.9:g.89707721_89707723delinsACT NCBI36
NG_007466.2:g.99546_99548delinsACT , LRG_311:g.99546_99548delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.766_768delinsACT ENSP00000514759.2:p.Glu256Thr
ENST00000710265.1:c.766_768delinsACT ENSP00000518161.1:p.Glu256Thr
ENST00000472832.3:c.766_768delinsACT ENSP00000483066.2:p.Glu256Thr
ENST00000688158.2:n.1501_1503delinsACT
ENST00000688922.2:c.*596_*598delinsACT ENSP00000508742.2:n.*596_*598delinsACT
ENST00000700021.1:c.721_723delinsACT ENSP00000514757.1:p.Glu241Thr
ENST00000700022.1:c.*105_*107delinsACT ENSP00000514758.1:n.*105_*107delinsACT
ENST00000700023.1:n.1924_1926delinsACT
ENST00000700024.1:n.2158_2160delinsACT
ENST00000700025.1:n.1535_1537delinsACT
ENST00000700026.1:n.403_405delinsACT
ENST00000700029.1:c.600_602delinsACT
ENST00000706954.1:c.766_768delinsACT ENSP00000516674.1:p.Glu256Thr
ENST00000706955.1:c.*801_*803delinsACT ENSP00000516675.1:n.*801_*803delinsACT
ENST00000686459.1:c.*352_*354delinsACT ENSP00000508909.1:n.*352_*354delinsACT
ENST00000688158.1:c.*877_*879delinsACT ENSP00000509254.1:n.*877_*879delinsACT
ENST00000688308.1:c.766_768delinsACT ENSP00000508752.1:p.Glu256Thr
ENST00000688922.1:c.687_689delinsACT
ENST00000693560.1:c.1285_1287delinsACT ENSP00000509861.1:p.Glu429Thr
ENST00000371953.8:c.766_768delinsACT MANE Select ENSP00000361021.3:p.Glu256Thr
ENST00000371953.7:c.766_768delinsACT ENSP00000361021.3:p.Glu256Thr
ENST00000472832.2:c.193_195delinsACT ENSP00000483066.1:p.Glu65Thr
NM_000314.5:c.766_768delinsACT NP_000305.3:p.Glu256Thr
NM_000314.6:c.766_768delinsACT NP_000305.3:p.Glu256Thr
NM_001304717.2:c.1285_1287delinsACT NP_001291646.2:p.Glu429Thr
NM_001304718.1:c.175_177delinsACT NP_001291647.1:p.Glu59Thr
XM_006717926.2:c.721_723delinsACT XP_006717989.1:p.Glu241Thr
XM_011539981.1:c.766_768delinsACT XP_011538283.1:p.Glu256Thr
XM_011539982.1:c.670_672delinsACT XP_011538284.1:p.Glu224Thr
XR_945791.1:n.1336_1338delinsACT
NM_000314.7:c.766_768delinsACT NP_000305.3:p.Glu256Thr
NM_001304717.5:c.1285_1287delinsACT NP_001291646.4:p.Glu429Thr
NM_001304718.2:c.175_177delinsACT NP_001291647.1:p.Glu59Thr
NM_000314.8:c.766_768delinsACT MANE Select NP_000305.3:p.Glu256Thr