Canonical Allele Identifier: CA891839859
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957960_87957961delinsTA , CM000672.2:g.87957960_87957961delinsTA GRCh38
NC_000010.10:g.89717717_89717718delinsTA , CM000672.1:g.89717717_89717718delinsTA GRCh37
NC_000010.9:g.89707697_89707698delinsTA NCBI36
NG_007466.2:g.99522_99523delinsTA , LRG_311:g.99522_99523delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.742_743delinsTA ENSP00000514759.2:p.Pro248Tyr
ENST00000710265.1:c.742_743delinsTA ENSP00000518161.1:p.Pro248Tyr
ENST00000472832.3:c.742_743delinsTA ENSP00000483066.2:p.Pro248Tyr
ENST00000688158.2:n.1477_1478delinsTA
ENST00000688922.2:c.*572_*573delinsTA ENSP00000508742.2:n.*572_*573delinsTA
ENST00000700021.1:c.697_698delinsTA ENSP00000514757.1:p.Pro233Tyr
ENST00000700022.1:c.*81_*82delinsTA ENSP00000514758.1:n.*81_*82delinsTA
ENST00000700023.1:n.1900_1901delinsTA
ENST00000700024.1:n.2134_2135delinsTA
ENST00000700025.1:n.1511_1512delinsTA
ENST00000700026.1:n.379_380delinsTA
ENST00000700029.1:c.576_577delinsTA
ENST00000706954.1:c.742_743delinsTA ENSP00000516674.1:p.Pro248Tyr
ENST00000706955.1:c.*777_*778delinsTA ENSP00000516675.1:n.*777_*778delinsTA
ENST00000686459.1:c.*328_*329delinsTA ENSP00000508909.1:n.*328_*329delinsTA
ENST00000688158.1:c.*853_*854delinsTA ENSP00000509254.1:n.*853_*854delinsTA
ENST00000688308.1:c.742_743delinsTA ENSP00000508752.1:p.Pro248Tyr
ENST00000688922.1:c.663_664delinsTA
ENST00000693560.1:c.1261_1262delinsTA ENSP00000509861.1:p.Pro421Tyr
ENST00000371953.8:c.742_743delinsTA MANE Select ENSP00000361021.3:p.Pro248Tyr
ENST00000371953.7:c.742_743delinsTA ENSP00000361021.3:p.Pro248Tyr
ENST00000472832.2:c.169_170delinsTA ENSP00000483066.1:p.Pro57Tyr
NM_000314.5:c.742_743delinsTA NP_000305.3:p.Pro248Tyr
NM_000314.6:c.742_743delinsTA NP_000305.3:p.Pro248Tyr
NM_001304717.2:c.1261_1262delinsTA NP_001291646.2:p.Pro421Tyr
NM_001304718.1:c.151_152delinsTA NP_001291647.1:p.Pro51Tyr
XM_006717926.2:c.697_698delinsTA XP_006717989.1:p.Pro233Tyr
XM_011539981.1:c.742_743delinsTA XP_011538283.1:p.Pro248Tyr
XM_011539982.1:c.646_647delinsTA XP_011538284.1:p.Pro216Tyr
XR_945791.1:n.1312_1313delinsTA
NM_000314.7:c.742_743delinsTA NP_000305.3:p.Pro248Tyr
NM_001304717.5:c.1261_1262delinsTA NP_001291646.4:p.Pro421Tyr
NM_001304718.2:c.151_152delinsTA NP_001291647.1:p.Pro51Tyr
NM_000314.8:c.742_743delinsTA MANE Select NP_000305.3:p.Pro248Tyr