Canonical Allele Identifier: CA1926190030
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961000T= , CM000672.2:g.87961000T= GRCh38
NC_000010.10:g.89720757T= , CM000672.1:g.89720757T= GRCh37
NC_000010.9:g.89710737T= NCBI36
NG_007466.2:g.102562T= , LRG_311:g.102562T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1001T= ENSP00000514759.2:p.Ile334=
ENST00000710265.1:c.908T= ENSP00000518161.1:p.Ile303=
ENST00000472832.3:c.908T= ENSP00000483066.2:p.Ile303=
ENST00000688158.2:n.1643T=
ENST00000688922.2:c.*738T= ENSP00000508742.2:n.*738T=
ENST00000700021.1:c.863T= ENSP00000514757.1:p.Ile288=
ENST00000700022.1:c.*247T= ENSP00000514758.1:n.*247T=
ENST00000700023.1:n.2066T=
ENST00000700024.1:n.2300T=
ENST00000700025.1:n.1677T=
ENST00000700026.1:n.545T=
ENST00000706954.1:c.908T= ENSP00000516674.1:p.Ile303=
ENST00000706955.1:c.*943T= ENSP00000516675.1:n.*943T=
ENST00000686459.1:c.*494T= ENSP00000508909.1:n.*494T=
ENST00000688158.1:c.*1019T= ENSP00000509254.1:n.*1019T=
ENST00000688308.1:c.908T= ENSP00000508752.1:p.Ile303=
ENST00000688922.1:c.829T=
ENST00000693560.1:c.1427T= ENSP00000509861.1:p.Ile476=
ENST00000371953.8:c.908T= MANE Select ENSP00000361021.3:p.Ile303=
ENST00000371953.7:c.908T= ENSP00000361021.3:p.Ile303=
ENST00000472832.2:c.335T= ENSP00000483066.1:p.Ile112=
NM_000314.5:c.908T= NP_000305.3:p.Ile303=
NM_000314.6:c.908T= NP_000305.3:p.Ile303=
NM_001304717.2:c.1427T= NP_001291646.2:p.Ile476=
NM_001304718.1:c.317T= NP_001291647.1:p.Ile106=
XM_006717926.2:c.863T= XP_006717989.1:p.Ile288=
XM_011539981.1:c.908T= XP_011538283.1:p.Ile303=
XM_011539982.1:c.812T= XP_011538284.1:p.Ile271=
XR_945791.1:n.1478T=
NM_000314.7:c.908T= NP_000305.3:p.Ile303=
NM_001304717.5:c.1427T= NP_001291646.4:p.Ile476=
NM_001304718.2:c.317T= NP_001291647.1:p.Ile106=
NM_000314.8:c.908T= MANE Select NP_000305.3:p.Ile303=