Canonical Allele Identifier: CA891839935
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957976_87957977delinsAT , CM000672.2:g.87957976_87957977delinsAT GRCh38
NC_000010.10:g.89717733_89717734delinsAT , CM000672.1:g.89717733_89717734delinsAT GRCh37
NC_000010.9:g.89707713_89707714delinsAT NCBI36
NG_007466.2:g.99538_99539delinsAT , LRG_311:g.99538_99539delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.758_759delinsAT ENSP00000514759.2:p.Ile253Asn
ENST00000710265.1:c.758_759delinsAT ENSP00000518161.1:p.Ile253Asn
ENST00000472832.3:c.758_759delinsAT ENSP00000483066.2:p.Ile253Asn
ENST00000688158.2:n.1493_1494delinsAT
ENST00000688922.2:c.*588_*589delinsAT ENSP00000508742.2:n.*588_*589delinsAT
ENST00000700021.1:c.713_714delinsAT ENSP00000514757.1:p.Ile238Asn
ENST00000700022.1:c.*97_*98delinsAT ENSP00000514758.1:n.*97_*98delinsAT
ENST00000700023.1:n.1916_1917delinsAT
ENST00000700024.1:n.2150_2151delinsAT
ENST00000700025.1:n.1527_1528delinsAT
ENST00000700026.1:n.395_396delinsAT
ENST00000700029.1:c.592_593delinsAT
ENST00000706954.1:c.758_759delinsAT ENSP00000516674.1:p.Ile253Asn
ENST00000706955.1:c.*793_*794delinsAT ENSP00000516675.1:n.*793_*794delinsAT
ENST00000686459.1:c.*344_*345delinsAT ENSP00000508909.1:n.*344_*345delinsAT
ENST00000688158.1:c.*869_*870delinsAT ENSP00000509254.1:n.*869_*870delinsAT
ENST00000688308.1:c.758_759delinsAT ENSP00000508752.1:p.Ile253Asn
ENST00000688922.1:c.679_680delinsAT
ENST00000693560.1:c.1277_1278delinsAT ENSP00000509861.1:p.Ile426Asn
ENST00000371953.8:c.758_759delinsAT MANE Select ENSP00000361021.3:p.Ile253Asn
ENST00000371953.7:c.758_759delinsAT ENSP00000361021.3:p.Ile253Asn
ENST00000472832.2:c.185_186delinsAT ENSP00000483066.1:p.Ile62Asn
NM_000314.5:c.758_759delinsAT NP_000305.3:p.Ile253Asn
NM_000314.6:c.758_759delinsAT NP_000305.3:p.Ile253Asn
NM_001304717.2:c.1277_1278delinsAT NP_001291646.2:p.Ile426Asn
NM_001304718.1:c.167_168delinsAT NP_001291647.1:p.Ile56Asn
XM_006717926.2:c.713_714delinsAT XP_006717989.1:p.Ile238Asn
XM_011539981.1:c.758_759delinsAT XP_011538283.1:p.Ile253Asn
XM_011539982.1:c.662_663delinsAT XP_011538284.1:p.Ile221Asn
XR_945791.1:n.1328_1329delinsAT
NM_000314.7:c.758_759delinsAT NP_000305.3:p.Ile253Asn
NM_001304717.5:c.1277_1278delinsAT NP_001291646.4:p.Ile426Asn
NM_001304718.2:c.167_168delinsAT NP_001291647.1:p.Ile56Asn
NM_000314.8:c.758_759delinsAT MANE Select NP_000305.3:p.Ile253Asn