Canonical Allele Identifier: CA891839879
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957964_87957965delinsCT , CM000672.2:g.87957964_87957965delinsCT GRCh38
NC_000010.10:g.89717721_89717722delinsCT , CM000672.1:g.89717721_89717722delinsCT GRCh37
NC_000010.9:g.89707701_89707702delinsCT NCBI36
NG_007466.2:g.99526_99527delinsCT , LRG_311:g.99526_99527delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.746_747delinsCT ENSP00000514759.2:p.Val249Ala
ENST00000710265.1:c.746_747delinsCT ENSP00000518161.1:p.Val249Ala
ENST00000472832.3:c.746_747delinsCT ENSP00000483066.2:p.Val249Ala
ENST00000688158.2:n.1481_1482delinsCT
ENST00000688922.2:c.*576_*577delinsCT ENSP00000508742.2:n.*576_*577delinsCT
ENST00000700021.1:c.701_702delinsCT ENSP00000514757.1:p.Val234Ala
ENST00000700022.1:c.*85_*86delinsCT ENSP00000514758.1:n.*85_*86delinsCT
ENST00000700023.1:n.1904_1905delinsCT
ENST00000700024.1:n.2138_2139delinsCT
ENST00000700025.1:n.1515_1516delinsCT
ENST00000700026.1:n.383_384delinsCT
ENST00000700029.1:c.580_581delinsCT
ENST00000706954.1:c.746_747delinsCT ENSP00000516674.1:p.Val249Ala
ENST00000706955.1:c.*781_*782delinsCT ENSP00000516675.1:n.*781_*782delinsCT
ENST00000686459.1:c.*332_*333delinsCT ENSP00000508909.1:n.*332_*333delinsCT
ENST00000688158.1:c.*857_*858delinsCT ENSP00000509254.1:n.*857_*858delinsCT
ENST00000688308.1:c.746_747delinsCT ENSP00000508752.1:p.Val249Ala
ENST00000688922.1:c.667_668delinsCT
ENST00000693560.1:c.1265_1266delinsCT ENSP00000509861.1:p.Val422Ala
ENST00000371953.8:c.746_747delinsCT MANE Select ENSP00000361021.3:p.Val249Ala
ENST00000371953.7:c.746_747delinsCT ENSP00000361021.3:p.Val249Ala
ENST00000472832.2:c.173_174delinsCT ENSP00000483066.1:p.Val58Ala
NM_000314.5:c.746_747delinsCT NP_000305.3:p.Val249Ala
NM_000314.6:c.746_747delinsCT NP_000305.3:p.Val249Ala
NM_001304717.2:c.1265_1266delinsCT NP_001291646.2:p.Val422Ala
NM_001304718.1:c.155_156delinsCT NP_001291647.1:p.Val52Ala
XM_006717926.2:c.701_702delinsCT XP_006717989.1:p.Val234Ala
XM_011539981.1:c.746_747delinsCT XP_011538283.1:p.Val249Ala
XM_011539982.1:c.650_651delinsCT XP_011538284.1:p.Val217Ala
XR_945791.1:n.1316_1317delinsCT
NM_000314.7:c.746_747delinsCT NP_000305.3:p.Val249Ala
NM_001304717.5:c.1265_1266delinsCT NP_001291646.4:p.Val422Ala
NM_001304718.2:c.155_156delinsCT NP_001291647.1:p.Val52Ala
NM_000314.8:c.746_747delinsCT MANE Select NP_000305.3:p.Val249Ala