Canonical Allele Identifier: CA2579927107
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894073_87894075del , CM000672.2:g.87894073_87894075del GRCh38
NC_000010.10:g.89653830_89653832del , CM000672.1:g.89653830_89653832del GRCh37
NC_000010.9:g.89643810_89643812del NCBI36
NG_007466.2:g.35635_35637del , LRG_311:g.35635_35637del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.128_130del ENSP00000514759.2:p.Glu43del
ENST00000710265.1:c.128_130del ENSP00000518161.1:p.Glu43del
ENST00000472832.3:c.128_130del ENSP00000483066.2:p.Glu43del
ENST00000688158.2:n.899+13635_899+13637del
ENST00000688922.2:c.128_130del ENSP00000508742.2:p.Glu43del
ENST00000700021.1:c.128_130del ENSP00000514757.1:p.Glu43del
ENST00000700022.1:c.128_130del ENSP00000514758.1:p.Glu43del
ENST00000706954.1:c.128_130del ENSP00000516674.1:p.Glu43del
ENST00000706955.1:c.*163_*165del ENSP00000516675.1:n.*163_*165del
ENST00000686459.1:c.128_130del ENSP00000508909.1:p.Glu43del
ENST00000688158.1:c.*275+13635_*275+13637del ENSP00000509254.1:n.*275+13635_*275+13637del
ENST00000688308.1:c.128_130del ENSP00000508752.1:p.Glu43del
ENST00000693560.1:c.647_649del ENSP00000509861.1:p.Glu216del
ENST00000371953.8:c.128_130del MANE Select ENSP00000361021.3:p.Glu43del
ENST00000371953.7:c.128_130del ENSP00000361021.3:p.Glu43del
ENST00000462694.1:n.130_132del
ENST00000610634.1:c.26_28del ENSP00000477517.1:p.Glu9del
NM_000314.5:c.128_130del NP_000305.3:p.Glu43del
NM_000314.6:c.128_130del NP_000305.3:p.Glu43del
NM_001304717.2:c.647_649del NP_001291646.2:p.Glu216del
NM_001304718.1:c.-578_-576del NP_001291647.1:n.-578_-576del
XM_006717926.2:c.128_130del XP_006717989.1:p.Glu43del
XM_011539981.1:c.128_130del XP_011538283.1:p.Glu43del
XM_011539982.1:c.68+13635_68+13637del XP_011538284.1:n.68+13635_68+13637del
XR_945789.1:n.840_842del
XR_945790.1:n.840_842del
XR_945791.1:n.840_842del
NM_000314.7:c.128_130del NP_000305.3:p.Glu43del
NM_001304717.5:c.647_649del NP_001291646.4:p.Glu216del
NM_001304718.2:c.-578_-576del NP_001291647.1:n.-578_-576del
NM_000314.8:c.128_130del MANE Select NP_000305.3:p.Glu43del