Canonical Allele Identifier: CA1926188585
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957968T= , CM000672.2:g.87957968T= GRCh38
NC_000010.10:g.89717725T= , CM000672.1:g.89717725T= GRCh37
NC_000010.9:g.89707705T= NCBI36
NG_007466.2:g.99530T= , LRG_311:g.99530T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.750T= ENSP00000514759.2:p.Cys250=
ENST00000710265.1:c.750T= ENSP00000518161.1:p.Cys250=
ENST00000472832.3:c.750T= ENSP00000483066.2:p.Cys250=
ENST00000688158.2:n.1485T=
ENST00000688922.2:c.*580T= ENSP00000508742.2:n.*580T=
ENST00000700021.1:c.705T= ENSP00000514757.1:p.Cys235=
ENST00000700022.1:c.*89T= ENSP00000514758.1:n.*89T=
ENST00000700023.1:n.1908T=
ENST00000700024.1:n.2142T=
ENST00000700025.1:n.1519T=
ENST00000700026.1:n.387T=
ENST00000700029.1:c.584T=
ENST00000706954.1:c.750T= ENSP00000516674.1:p.Cys250=
ENST00000706955.1:c.*785T= ENSP00000516675.1:n.*785T=
ENST00000686459.1:c.*336T= ENSP00000508909.1:n.*336T=
ENST00000688158.1:c.*861T= ENSP00000509254.1:n.*861T=
ENST00000688308.1:c.750T= ENSP00000508752.1:p.Cys250=
ENST00000688922.1:c.671T=
ENST00000693560.1:c.1269T= ENSP00000509861.1:p.Cys423=
ENST00000371953.8:c.750T= MANE Select ENSP00000361021.3:p.Cys250=
ENST00000371953.7:c.750T= ENSP00000361021.3:p.Cys250=
ENST00000472832.2:c.177T= ENSP00000483066.1:p.Cys59=
NM_000314.5:c.750T= NP_000305.3:p.Cys250=
NM_000314.6:c.750T= NP_000305.3:p.Cys250=
NM_001304717.2:c.1269T= NP_001291646.2:p.Cys423=
NM_001304718.1:c.159T= NP_001291647.1:p.Cys53=
XM_006717926.2:c.705T= XP_006717989.1:p.Cys235=
XM_011539981.1:c.750T= XP_011538283.1:p.Cys250=
XM_011539982.1:c.654T= XP_011538284.1:p.Cys218=
XR_945791.1:n.1320T=
NM_000314.7:c.750T= NP_000305.3:p.Cys250=
NM_001304717.5:c.1269T= NP_001291646.4:p.Cys423=
NM_001304718.2:c.159T= NP_001291647.1:p.Cys53=
NM_000314.8:c.750T= MANE Select NP_000305.3:p.Cys250=