Canonical Allele Identifier: CA891840937
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958002_87958003delinsGT , CM000672.2:g.87958002_87958003delinsGT GRCh38
NC_000010.10:g.89717759_89717760delinsGT , CM000672.1:g.89717759_89717760delinsGT GRCh37
NC_000010.9:g.89707739_89707740delinsGT NCBI36
NG_007466.2:g.99564_99565delinsGT , LRG_311:g.99564_99565delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.784_785delinsGT ENSP00000514759.2:p.Asn262Val
ENST00000710265.1:c.784_785delinsGT ENSP00000518161.1:p.Asn262Val
ENST00000472832.3:c.784_785delinsGT ENSP00000483066.2:p.Asn262Val
ENST00000688158.2:n.1519_1520delinsGT
ENST00000688922.2:c.*614_*615delinsGT ENSP00000508742.2:n.*614_*615delinsGT
ENST00000700021.1:c.739_740delinsGT ENSP00000514757.1:p.Asn247Val
ENST00000700022.1:c.*123_*124delinsGT ENSP00000514758.1:n.*123_*124delinsGT
ENST00000700023.1:n.1942_1943delinsGT
ENST00000700024.1:n.2176_2177delinsGT
ENST00000700025.1:n.1553_1554delinsGT
ENST00000700026.1:n.421_422delinsGT
ENST00000700029.1:c.618_619delinsGT
ENST00000706954.1:c.784_785delinsGT ENSP00000516674.1:p.Asn262Val
ENST00000706955.1:c.*819_*820delinsGT ENSP00000516675.1:n.*819_*820delinsGT
ENST00000686459.1:c.*370_*371delinsGT ENSP00000508909.1:n.*370_*371delinsGT
ENST00000688158.1:c.*895_*896delinsGT ENSP00000509254.1:n.*895_*896delinsGT
ENST00000688308.1:c.784_785delinsGT ENSP00000508752.1:p.Asn262Val
ENST00000688922.1:c.705_706delinsGT
ENST00000693560.1:c.1303_1304delinsGT ENSP00000509861.1:p.Asn435Val
ENST00000371953.8:c.784_785delinsGT MANE Select ENSP00000361021.3:p.Asn262Val
ENST00000371953.7:c.784_785delinsGT ENSP00000361021.3:p.Asn262Val
ENST00000472832.2:c.211_212delinsGT ENSP00000483066.1:p.Asn71Val
NM_000314.5:c.784_785delinsGT NP_000305.3:p.Asn262Val
NM_000314.6:c.784_785delinsGT NP_000305.3:p.Asn262Val
NM_001304717.2:c.1303_1304delinsGT NP_001291646.2:p.Asn435Val
NM_001304718.1:c.193_194delinsGT NP_001291647.1:p.Asn65Val
XM_006717926.2:c.739_740delinsGT XP_006717989.1:p.Asn247Val
XM_011539981.1:c.784_785delinsGT XP_011538283.1:p.Asn262Val
XM_011539982.1:c.688_689delinsGT XP_011538284.1:p.Asn230Val
XR_945791.1:n.1354_1355delinsGT
NM_000314.7:c.784_785delinsGT NP_000305.3:p.Asn262Val
NM_001304717.5:c.1303_1304delinsGT NP_001291646.4:p.Asn435Val
NM_001304718.2:c.193_194delinsGT NP_001291647.1:p.Asn65Val
NM_000314.8:c.784_785delinsGT MANE Select NP_000305.3:p.Asn262Val