Canonical Allele Identifier: CA891839877
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957964_87957965delinsAA , CM000672.2:g.87957964_87957965delinsAA GRCh38
NC_000010.10:g.89717721_89717722delinsAA , CM000672.1:g.89717721_89717722delinsAA GRCh37
NC_000010.9:g.89707701_89707702delinsAA NCBI36
NG_007466.2:g.99526_99527delinsAA , LRG_311:g.99526_99527delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.746_747delinsAA ENSP00000514759.2:p.Val249Glu
ENST00000710265.1:c.746_747delinsAA ENSP00000518161.1:p.Val249Glu
ENST00000472832.3:c.746_747delinsAA ENSP00000483066.2:p.Val249Glu
ENST00000688158.2:n.1481_1482delinsAA
ENST00000688922.2:c.*576_*577delinsAA ENSP00000508742.2:n.*576_*577delinsAA
ENST00000700021.1:c.701_702delinsAA ENSP00000514757.1:p.Val234Glu
ENST00000700022.1:c.*85_*86delinsAA ENSP00000514758.1:n.*85_*86delinsAA
ENST00000700023.1:n.1904_1905delinsAA
ENST00000700024.1:n.2138_2139delinsAA
ENST00000700025.1:n.1515_1516delinsAA
ENST00000700026.1:n.383_384delinsAA
ENST00000700029.1:c.580_581delinsAA
ENST00000706954.1:c.746_747delinsAA ENSP00000516674.1:p.Val249Glu
ENST00000706955.1:c.*781_*782delinsAA ENSP00000516675.1:n.*781_*782delinsAA
ENST00000686459.1:c.*332_*333delinsAA ENSP00000508909.1:n.*332_*333delinsAA
ENST00000688158.1:c.*857_*858delinsAA ENSP00000509254.1:n.*857_*858delinsAA
ENST00000688308.1:c.746_747delinsAA ENSP00000508752.1:p.Val249Glu
ENST00000688922.1:c.667_668delinsAA
ENST00000693560.1:c.1265_1266delinsAA ENSP00000509861.1:p.Val422Glu
ENST00000371953.8:c.746_747delinsAA MANE Select ENSP00000361021.3:p.Val249Glu
ENST00000371953.7:c.746_747delinsAA ENSP00000361021.3:p.Val249Glu
ENST00000472832.2:c.173_174delinsAA ENSP00000483066.1:p.Val58Glu
NM_000314.5:c.746_747delinsAA NP_000305.3:p.Val249Glu
NM_000314.6:c.746_747delinsAA NP_000305.3:p.Val249Glu
NM_001304717.2:c.1265_1266delinsAA NP_001291646.2:p.Val422Glu
NM_001304718.1:c.155_156delinsAA NP_001291647.1:p.Val52Glu
XM_006717926.2:c.701_702delinsAA XP_006717989.1:p.Val234Glu
XM_011539981.1:c.746_747delinsAA XP_011538283.1:p.Val249Glu
XM_011539982.1:c.650_651delinsAA XP_011538284.1:p.Val217Glu
XR_945791.1:n.1316_1317delinsAA
NM_000314.7:c.746_747delinsAA NP_000305.3:p.Val249Glu
NM_001304717.5:c.1265_1266delinsAA NP_001291646.4:p.Val422Glu
NM_001304718.2:c.155_156delinsAA NP_001291647.1:p.Val52Glu
NM_000314.8:c.746_747delinsAA MANE Select NP_000305.3:p.Val249Glu