Canonical Allele Identifier: CA891835135
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894075_87894077delinsCAA , CM000672.2:g.87894075_87894077delinsCAA GRCh38
NC_000010.10:g.89653832_89653834delinsCAA , CM000672.1:g.89653832_89653834delinsCAA GRCh37
NC_000010.9:g.89643812_89643814delinsCAA NCBI36
NG_007466.2:g.35637_35639delinsCAA , LRG_311:g.35637_35639delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.130_132delinsCAA ENSP00000514759.2:p.Gly44Gln
ENST00000710265.1:c.130_132delinsCAA ENSP00000518161.1:p.Gly44Gln
ENST00000472832.3:c.130_132delinsCAA ENSP00000483066.2:p.Gly44Gln
ENST00000688158.2:n.899+13637_899+13639delinsCAA
ENST00000688922.2:c.130_132delinsCAA ENSP00000508742.2:p.Gly44Gln
ENST00000700021.1:c.130_132delinsCAA ENSP00000514757.1:p.Gly44Gln
ENST00000700022.1:c.130_132delinsCAA ENSP00000514758.1:p.Gly44Gln
ENST00000706954.1:c.130_132delinsCAA ENSP00000516674.1:p.Gly44Gln
ENST00000706955.1:c.*165_*167delinsCAA ENSP00000516675.1:n.*165_*167delinsCAA
ENST00000686459.1:c.130_132delinsCAA ENSP00000508909.1:p.Gly44Gln
ENST00000688158.1:c.*275+13637_*275+13639delinsCAA ENSP00000509254.1:n.*275+13637_*275+13639delinsCAA
ENST00000688308.1:c.130_132delinsCAA ENSP00000508752.1:p.Gly44Gln
ENST00000693560.1:c.649_651delinsCAA ENSP00000509861.1:p.Gly217Gln
ENST00000371953.8:c.130_132delinsCAA MANE Select ENSP00000361021.3:p.Gly44Gln
ENST00000371953.7:c.130_132delinsCAA ENSP00000361021.3:p.Gly44Gln
ENST00000462694.1:n.132_134delinsCAA
ENST00000610634.1:c.28_30delinsCAA ENSP00000477517.1:p.Gly10Gln
NM_000314.5:c.130_132delinsCAA NP_000305.3:p.Gly44Gln
NM_000314.6:c.130_132delinsCAA NP_000305.3:p.Gly44Gln
NM_001304717.2:c.649_651delinsCAA NP_001291646.2:p.Gly217Gln
NM_001304718.1:c.-576_-574delinsCAA NP_001291647.1:n.-576_-574delinsCAA
XM_006717926.2:c.130_132delinsCAA XP_006717989.1:p.Gly44Gln
XM_011539981.1:c.130_132delinsCAA XP_011538283.1:p.Gly44Gln
XM_011539982.1:c.68+13637_68+13639delinsCAA XP_011538284.1:n.68+13637_68+13639delinsCAA
XR_945789.1:n.842_844delinsCAA
XR_945790.1:n.842_844delinsCAA
XR_945791.1:n.842_844delinsCAA
NM_000314.7:c.130_132delinsCAA NP_000305.3:p.Gly44Gln
NM_001304717.5:c.649_651delinsCAA NP_001291646.4:p.Gly217Gln
NM_001304718.2:c.-576_-574delinsCAA NP_001291647.1:n.-576_-574delinsCAA
NM_000314.8:c.130_132delinsCAA MANE Select NP_000305.3:p.Gly44Gln