Canonical Allele Identifier: CA1926157268
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894080A= , CM000672.2:g.87894080A= GRCh38
NC_000010.10:g.89653837A= , CM000672.1:g.89653837A= GRCh37
NC_000010.9:g.89643817A= NCBI36
NG_007466.2:g.35642A= , LRG_311:g.35642A=

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.135A= ENSP00000514759.2:p.Val45=
ENST00000710265.1:c.135A= ENSP00000518161.1:p.Val45=
ENST00000472832.3:c.135A= ENSP00000483066.2:p.Val45=
ENST00000688158.2:n.899+13642A=
ENST00000688922.2:c.135A= ENSP00000508742.2:p.Val45=
ENST00000700021.1:c.135A= ENSP00000514757.1:p.Val45=
ENST00000700022.1:c.135A= ENSP00000514758.1:p.Val45=
ENST00000706954.1:c.135A= ENSP00000516674.1:p.Val45=
ENST00000706955.1:c.*170A= ENSP00000516675.1:n.*170A=
ENST00000686459.1:c.135A= ENSP00000508909.1:p.Val45=
ENST00000688158.1:c.*275+13642A= ENSP00000509254.1:n.*275+13642A=
ENST00000688308.1:c.135A= ENSP00000508752.1:p.Val45=
ENST00000688922.1:c.4A=
ENST00000693560.1:c.654A= ENSP00000509861.1:p.Val218=
ENST00000371953.8:c.135A= MANE Select ENSP00000361021.3:p.Val45=
ENST00000371953.7:c.135A= ENSP00000361021.3:p.Val45=
ENST00000462694.1:n.137A=
ENST00000610634.1:c.33A= ENSP00000477517.1:p.Val11=
NM_000314.5:c.135A= NP_000305.3:p.Val45=
NM_000314.6:c.135A= NP_000305.3:p.Val45=
NM_001304717.2:c.654A= NP_001291646.2:p.Val218=
NM_001304718.1:c.-571A= NP_001291647.1:n.-571A=
XM_006717926.2:c.135A= XP_006717989.1:p.Val45=
XM_011539981.1:c.135A= XP_011538283.1:p.Val45=
XM_011539982.1:c.68+13642A= XP_011538284.1:n.68+13642A=
XR_945789.1:n.847A=
XR_945790.1:n.847A=
XR_945791.1:n.847A=
NM_000314.7:c.135A= NP_000305.3:p.Val45=
NM_001304717.5:c.654A= NP_001291646.4:p.Val218=
NM_001304718.2:c.-571A= NP_001291647.1:n.-571A=
NM_000314.8:c.135A= MANE Select NP_000305.3:p.Val45=