Canonical Allele Identifier: CA891834544
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894030_87894032delinsGAA , CM000672.2:g.87894030_87894032delinsGAA GRCh38
NC_000010.10:g.89653787_89653789delinsGAA , CM000672.1:g.89653787_89653789delinsGAA GRCh37
NC_000010.9:g.89643767_89643769delinsGAA NCBI36
NG_007466.2:g.35592_35594delinsGAA , LRG_311:g.35592_35594delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.85_87delinsGAA ENSP00000514759.2:p.Tyr29Glu
ENST00000710265.1:c.85_87delinsGAA ENSP00000518161.1:p.Tyr29Glu
ENST00000472832.3:c.85_87delinsGAA ENSP00000483066.2:p.Tyr29Glu
ENST00000688158.2:n.899+13592_899+13594delinsGAA
ENST00000688922.2:c.85_87delinsGAA ENSP00000508742.2:p.Tyr29Glu
ENST00000700021.1:c.85_87delinsGAA ENSP00000514757.1:p.Tyr29Glu
ENST00000700022.1:c.85_87delinsGAA ENSP00000514758.1:p.Tyr29Glu
ENST00000706954.1:c.85_87delinsGAA ENSP00000516674.1:p.Tyr29Glu
ENST00000706955.1:c.*120_*122delinsGAA ENSP00000516675.1:n.*120_*122delinsGAA
ENST00000686459.1:c.85_87delinsGAA ENSP00000508909.1:p.Tyr29Glu
ENST00000688158.1:c.*275+13592_*275+13594delinsGAA ENSP00000509254.1:n.*275+13592_*275+13594delinsGAA
ENST00000688308.1:c.85_87delinsGAA ENSP00000508752.1:p.Tyr29Glu
ENST00000693560.1:c.604_606delinsGAA ENSP00000509861.1:p.Tyr202Glu
ENST00000371953.8:c.85_87delinsGAA MANE Select ENSP00000361021.3:p.Tyr29Glu
ENST00000371953.7:c.85_87delinsGAA ENSP00000361021.3:p.Tyr29Glu
ENST00000462694.1:n.87_89delinsGAA
ENST00000610634.1:c.-18_-16delinsGAA ENSP00000477517.1:n.-18_-16delinsGAA
NM_000314.5:c.85_87delinsGAA NP_000305.3:p.Tyr29Glu
NM_000314.6:c.85_87delinsGAA NP_000305.3:p.Tyr29Glu
NM_001304717.2:c.604_606delinsGAA NP_001291646.2:p.Tyr202Glu
NM_001304718.1:c.-621_-619delinsGAA NP_001291647.1:n.-621_-619delinsGAA
XM_006717926.2:c.85_87delinsGAA XP_006717989.1:p.Tyr29Glu
XM_011539981.1:c.85_87delinsGAA XP_011538283.1:p.Tyr29Glu
XM_011539982.1:c.68+13592_68+13594delinsGAA XP_011538284.1:n.68+13592_68+13594delinsGAA
XR_945789.1:n.797_799delinsGAA
XR_945790.1:n.797_799delinsGAA
XR_945791.1:n.797_799delinsGAA
NM_000314.7:c.85_87delinsGAA NP_000305.3:p.Tyr29Glu
NM_001304717.5:c.604_606delinsGAA NP_001291646.4:p.Tyr202Glu
NM_001304718.2:c.-621_-619delinsGAA NP_001291647.1:n.-621_-619delinsGAA
NM_000314.8:c.85_87delinsGAA MANE Select NP_000305.3:p.Tyr29Glu