Canonical Allele Identifier: CA16609232
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87864513_87864514dup , CM000672.2:g.87864513_87864514dup GRCh38
NC_000010.10:g.89624270_89624271dup , CM000672.1:g.89624270_89624271dup GRCh37
NC_000010.9:g.89614250_89614251dup NCBI36
NG_007466.2:g.6075_6076dup , LRG_311:g.6075_6076dup
NG_033079.1:g.3926_3927dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.44_45dup ENSP00000514759.2:p.Tyr16AspfsTer9
ENST00000710265.1:c.44_45dup ENSP00000518161.1:p.Tyr16AspfsTer9
ENST00000472832.3:c.44_45dup ENSP00000483066.2:p.Tyr16AspfsTer9
ENST00000688922.2:c.44_45dup ENSP00000508742.2:p.Tyr16AspfsTer9
ENST00000700021.1:c.44_45dup ENSP00000514757.1:p.Tyr16AspfsTer9
ENST00000700022.1:c.44_45dup ENSP00000514758.1:p.Tyr16AspfsTer9
ENST00000706954.1:c.44_45dup ENSP00000516674.1:p.Tyr16AspfsTer9
ENST00000706955.1:c.44_45dup ENSP00000516675.1:p.Tyr16AspfsTer9
ENST00000686459.1:c.44_45dup ENSP00000508909.1:p.Tyr16AspfsTer9
ENST00000688158.1:c.44_45dup ENSP00000509254.1:p.Tyr16AspfsTer9
ENST00000688308.1:c.44_45dup ENSP00000508752.1:p.Tyr16AspfsTer9
ENST00000693560.1:c.563_564dup ENSP00000509861.1:p.Tyr189AspfsTer9
ENST00000371953.8:c.44_45dup MANE Select ENSP00000361021.3:p.Tyr16AspfsTer9
ENST00000371953.7:c.44_45dup ENSP00000361021.3:p.Tyr16AspfsTer9
ENST00000462694.1:n.46_47dup
ENST00000487939.1:n.65_66dup
ENST00000610634.1:c.-59_-58dup ENSP00000477517.1:n.-59_-58dup
ENST00000618586.1:n.13_14dup
NM_000314.5:c.44_45dup NP_000305.3:p.Tyr16AspfsTer9
NM_000314.6:c.44_45dup NP_000305.3:p.Tyr16AspfsTer9
NM_001304717.2:c.563_564dup NP_001291646.2:p.Tyr189AspfsTer9
NM_001304718.1:c.-662_-661dup NP_001291647.1:n.-662_-661dup
XM_006717926.2:c.44_45dup XP_006717989.1:p.Tyr16AspfsTer9
XM_011539981.1:c.44_45dup XP_011538283.1:p.Tyr16AspfsTer9
XR_945789.1:n.756_757dup
XR_945790.1:n.756_757dup
XR_945791.1:n.756_757dup
NM_000314.7:c.44_45dup NP_000305.3:p.Tyr16AspfsTer9
NM_001304717.5:c.563_564dup NP_001291646.4:p.Tyr189AspfsTer9
NM_001304718.2:c.-662_-661dup NP_001291647.1:n.-662_-661dup
NM_000314.8:c.44_45dup MANE Select NP_000305.3:p.Tyr16AspfsTer9