Canonical Allele Identifier: CA891835303
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894085_87894086delinsAA , CM000672.2:g.87894085_87894086delinsAA GRCh38
NC_000010.10:g.89653842_89653843delinsAA , CM000672.1:g.89653842_89653843delinsAA GRCh37
NC_000010.9:g.89643822_89643823delinsAA NCBI36
NG_007466.2:g.35647_35648delinsAA , LRG_311:g.35647_35648delinsAA

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.140_141delinsAA ENSP00000514759.2:p.Arg47Lys
ENST00000710265.1:c.140_141delinsAA ENSP00000518161.1:p.Arg47Lys
ENST00000472832.3:c.140_141delinsAA ENSP00000483066.2:p.Arg47Lys
ENST00000688158.2:n.899+13647_899+13648delinsAA
ENST00000688922.2:c.140_141delinsAA ENSP00000508742.2:p.Arg47Lys
ENST00000700021.1:c.140_141delinsAA ENSP00000514757.1:p.Arg47Lys
ENST00000700022.1:c.140_141delinsAA ENSP00000514758.1:p.Arg47Lys
ENST00000706954.1:c.140_141delinsAA ENSP00000516674.1:p.Arg47Lys
ENST00000706955.1:c.*175_*176delinsAA ENSP00000516675.1:n.*175_*176delinsAA
ENST00000686459.1:c.140_141delinsAA ENSP00000508909.1:p.Arg47Lys
ENST00000688158.1:c.*275+13647_*275+13648delinsAA ENSP00000509254.1:n.*275+13647_*275+13648...
ENST00000688308.1:c.140_141delinsAA ENSP00000508752.1:p.Arg47Lys
ENST00000688922.1:c.9_10delinsAA
ENST00000693560.1:c.659_660delinsAA ENSP00000509861.1:p.Arg220Lys
ENST00000371953.8:c.140_141delinsAA MANE Select ENSP00000361021.3:p.Arg47Lys
ENST00000371953.7:c.140_141delinsAA ENSP00000361021.3:p.Arg47Lys
ENST00000462694.1:n.142_143delinsAA
ENST00000610634.1:c.38_39delinsAA ENSP00000477517.1:p.Arg13Lys
NM_000314.5:c.140_141delinsAA NP_000305.3:p.Arg47Lys
NM_000314.6:c.140_141delinsAA NP_000305.3:p.Arg47Lys
NM_001304717.2:c.659_660delinsAA NP_001291646.2:p.Arg220Lys
NM_001304718.1:c.-566_-565delinsAA NP_001291647.1:n.-566_-565delinsAA
XM_006717926.2:c.140_141delinsAA XP_006717989.1:p.Arg47Lys
XM_011539981.1:c.140_141delinsAA XP_011538283.1:p.Arg47Lys
XM_011539982.1:c.68+13647_68+13648delinsAA XP_011538284.1:n.68+13647_68+13648delinsA...
XR_945789.1:n.852_853delinsAA
XR_945790.1:n.852_853delinsAA
XR_945791.1:n.852_853delinsAA
NM_000314.7:c.140_141delinsAA NP_000305.3:p.Arg47Lys
NM_001304717.5:c.659_660delinsAA NP_001291646.4:p.Arg220Lys
NM_001304718.2:c.-566_-565delinsAA NP_001291647.1:n.-566_-565delinsAA
NM_000314.8:c.140_141delinsAA MANE Select NP_000305.3:p.Arg47Lys