Canonical Allele Identifier: CA891840942
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958002_87958003delinsGC , CM000672.2:g.87958002_87958003delinsGC GRCh38
NC_000010.10:g.89717759_89717760delinsGC , CM000672.1:g.89717759_89717760delinsGC GRCh37
NC_000010.9:g.89707739_89707740delinsGC NCBI36
NG_007466.2:g.99564_99565delinsGC , LRG_311:g.99564_99565delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.784_785delinsGC ENSP00000514759.2:p.Asn262Ala
ENST00000710265.1:c.784_785delinsGC ENSP00000518161.1:p.Asn262Ala
ENST00000472832.3:c.784_785delinsGC ENSP00000483066.2:p.Asn262Ala
ENST00000688158.2:n.1519_1520delinsGC
ENST00000688922.2:c.*614_*615delinsGC ENSP00000508742.2:n.*614_*615delinsGC
ENST00000700021.1:c.739_740delinsGC ENSP00000514757.1:p.Asn247Ala
ENST00000700022.1:c.*123_*124delinsGC ENSP00000514758.1:n.*123_*124delinsGC
ENST00000700023.1:n.1942_1943delinsGC
ENST00000700024.1:n.2176_2177delinsGC
ENST00000700025.1:n.1553_1554delinsGC
ENST00000700026.1:n.421_422delinsGC
ENST00000700029.1:c.618_619delinsGC
ENST00000706954.1:c.784_785delinsGC ENSP00000516674.1:p.Asn262Ala
ENST00000706955.1:c.*819_*820delinsGC ENSP00000516675.1:n.*819_*820delinsGC
ENST00000686459.1:c.*370_*371delinsGC ENSP00000508909.1:n.*370_*371delinsGC
ENST00000688158.1:c.*895_*896delinsGC ENSP00000509254.1:n.*895_*896delinsGC
ENST00000688308.1:c.784_785delinsGC ENSP00000508752.1:p.Asn262Ala
ENST00000688922.1:c.705_706delinsGC
ENST00000693560.1:c.1303_1304delinsGC ENSP00000509861.1:p.Asn435Ala
ENST00000371953.8:c.784_785delinsGC MANE Select ENSP00000361021.3:p.Asn262Ala
ENST00000371953.7:c.784_785delinsGC ENSP00000361021.3:p.Asn262Ala
ENST00000472832.2:c.211_212delinsGC ENSP00000483066.1:p.Asn71Ala
NM_000314.5:c.784_785delinsGC NP_000305.3:p.Asn262Ala
NM_000314.6:c.784_785delinsGC NP_000305.3:p.Asn262Ala
NM_001304717.2:c.1303_1304delinsGC NP_001291646.2:p.Asn435Ala
NM_001304718.1:c.193_194delinsGC NP_001291647.1:p.Asn65Ala
XM_006717926.2:c.739_740delinsGC XP_006717989.1:p.Asn247Ala
XM_011539981.1:c.784_785delinsGC XP_011538283.1:p.Asn262Ala
XM_011539982.1:c.688_689delinsGC XP_011538284.1:p.Asn230Ala
XR_945791.1:n.1354_1355delinsGC
NM_000314.7:c.784_785delinsGC NP_000305.3:p.Asn262Ala
NM_001304717.5:c.1303_1304delinsGC NP_001291646.4:p.Asn435Ala
NM_001304718.2:c.193_194delinsGC NP_001291647.1:p.Asn65Ala
NM_000314.8:c.784_785delinsGC MANE Select NP_000305.3:p.Asn262Ala