Canonical Allele Identifier: CA470669850
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM5026
MyVariant Identifiers: chr10:g.89717717_89717718insA (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957960_87957961insA , CM000672.2:g.87957960_87957961insA GRCh38
NC_000010.10:g.89717717_89717718insA , CM000672.1:g.89717717_89717718insA GRCh37
NC_000010.9:g.89707697_89707698insA NCBI36
NG_007466.2:g.99522_99523insA , LRG_311:g.99522_99523insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.742_743insA ENSP00000514759.2:p.Pro248HisfsTer5
ENST00000710265.1:c.742_743insA ENSP00000518161.1:p.Pro248HisfsTer5
ENST00000472832.3:c.742_743insA ENSP00000483066.2:p.Pro248HisfsTer5
ENST00000688158.2:n.1477_1478insA
ENST00000688922.2:c.*572_*573insA ENSP00000508742.2:n.*572_*573insA
ENST00000700021.1:c.697_698insA ENSP00000514757.1:p.Pro233HisfsTer5
ENST00000700022.1:c.*81_*82insA ENSP00000514758.1:n.*81_*82insA
ENST00000700023.1:n.1900_1901insA
ENST00000700024.1:n.2134_2135insA
ENST00000700025.1:n.1511_1512insA
ENST00000700026.1:n.379_380insA
ENST00000700029.1:c.576_577insA
ENST00000706954.1:c.742_743insA ENSP00000516674.1:p.Pro248HisfsTer5
ENST00000706955.1:c.*777_*778insA ENSP00000516675.1:n.*777_*778insA
ENST00000686459.1:c.*328_*329insA ENSP00000508909.1:n.*328_*329insA
ENST00000688158.1:c.*853_*854insA ENSP00000509254.1:n.*853_*854insA
ENST00000688308.1:c.742_743insA ENSP00000508752.1:p.Pro248HisfsTer5
ENST00000688922.1:c.663_664insA
ENST00000693560.1:c.1261_1262insA ENSP00000509861.1:p.Pro421HisfsTer5
ENST00000371953.8:c.742_743insA MANE Select ENSP00000361021.3:p.Pro248HisfsTer5
ENST00000371953.7:c.742_743insA ENSP00000361021.3:p.Pro248HisfsTer5
ENST00000472832.2:c.169_170insA ENSP00000483066.1:p.Pro57HisfsTer5
NM_000314.5:c.742_743insA NP_000305.3:p.Pro248HisfsTer5
NM_000314.6:c.742_743insA NP_000305.3:p.Pro248HisfsTer5
NM_001304717.2:c.1261_1262insA NP_001291646.2:p.Pro421HisfsTer5
NM_001304718.1:c.151_152insA NP_001291647.1:p.Pro51HisfsTer5
XM_006717926.2:c.697_698insA XP_006717989.1:p.Pro233HisfsTer5
XM_011539981.1:c.742_743insA XP_011538283.1:p.Pro248HisfsTer5
XM_011539982.1:c.646_647insA XP_011538284.1:p.Pro216HisfsTer5
XR_945791.1:n.1312_1313insA
NM_000314.7:c.742_743insA NP_000305.3:p.Pro248HisfsTer5
NM_001304717.5:c.1261_1262insA NP_001291646.4:p.Pro421HisfsTer5
NM_001304718.2:c.151_152insA NP_001291647.1:p.Pro51HisfsTer5
NM_000314.8:c.742_743insA MANE Select NP_000305.3:p.Pro248HisfsTer5
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