Canonical Allele Identifier: CA891839856
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957960_87957961delinsAT , CM000672.2:g.87957960_87957961delinsAT GRCh38
NC_000010.10:g.89717717_89717718delinsAT , CM000672.1:g.89717717_89717718delinsAT GRCh37
NC_000010.9:g.89707697_89707698delinsAT NCBI36
NG_007466.2:g.99522_99523delinsAT , LRG_311:g.99522_99523delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.742_743delinsAT ENSP00000514759.2:p.Pro248Ile
ENST00000710265.1:c.742_743delinsAT ENSP00000518161.1:p.Pro248Ile
ENST00000472832.3:c.742_743delinsAT ENSP00000483066.2:p.Pro248Ile
ENST00000688158.2:n.1477_1478delinsAT
ENST00000688922.2:c.*572_*573delinsAT ENSP00000508742.2:n.*572_*573delinsAT
ENST00000700021.1:c.697_698delinsAT ENSP00000514757.1:p.Pro233Ile
ENST00000700022.1:c.*81_*82delinsAT ENSP00000514758.1:n.*81_*82delinsAT
ENST00000700023.1:n.1900_1901delinsAT
ENST00000700024.1:n.2134_2135delinsAT
ENST00000700025.1:n.1511_1512delinsAT
ENST00000700026.1:n.379_380delinsAT
ENST00000700029.1:c.576_577delinsAT
ENST00000706954.1:c.742_743delinsAT ENSP00000516674.1:p.Pro248Ile
ENST00000706955.1:c.*777_*778delinsAT ENSP00000516675.1:n.*777_*778delinsAT
ENST00000686459.1:c.*328_*329delinsAT ENSP00000508909.1:n.*328_*329delinsAT
ENST00000688158.1:c.*853_*854delinsAT ENSP00000509254.1:n.*853_*854delinsAT
ENST00000688308.1:c.742_743delinsAT ENSP00000508752.1:p.Pro248Ile
ENST00000688922.1:c.663_664delinsAT
ENST00000693560.1:c.1261_1262delinsAT ENSP00000509861.1:p.Pro421Ile
ENST00000371953.8:c.742_743delinsAT MANE Select ENSP00000361021.3:p.Pro248Ile
ENST00000371953.7:c.742_743delinsAT ENSP00000361021.3:p.Pro248Ile
ENST00000472832.2:c.169_170delinsAT ENSP00000483066.1:p.Pro57Ile
NM_000314.5:c.742_743delinsAT NP_000305.3:p.Pro248Ile
NM_000314.6:c.742_743delinsAT NP_000305.3:p.Pro248Ile
NM_001304717.2:c.1261_1262delinsAT NP_001291646.2:p.Pro421Ile
NM_001304718.1:c.151_152delinsAT NP_001291647.1:p.Pro51Ile
XM_006717926.2:c.697_698delinsAT XP_006717989.1:p.Pro233Ile
XM_011539981.1:c.742_743delinsAT XP_011538283.1:p.Pro248Ile
XM_011539982.1:c.646_647delinsAT XP_011538284.1:p.Pro216Ile
XR_945791.1:n.1312_1313delinsAT
NM_000314.7:c.742_743delinsAT NP_000305.3:p.Pro248Ile
NM_001304717.5:c.1261_1262delinsAT NP_001291646.4:p.Pro421Ile
NM_001304718.2:c.151_152delinsAT NP_001291647.1:p.Pro51Ile
NM_000314.8:c.742_743delinsAT MANE Select NP_000305.3:p.Pro248Ile