Canonical Allele Identifier: CA1926188601
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957982T= , CM000672.2:g.87957982T= GRCh38
NC_000010.10:g.89717739T= , CM000672.1:g.89717739T= GRCh37
NC_000010.9:g.89707719T= NCBI36
NG_007466.2:g.99544T= , LRG_311:g.99544T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.764T= ENSP00000514759.2:p.Val255=
ENST00000710265.1:c.764T= ENSP00000518161.1:p.Val255=
ENST00000472832.3:c.764T= ENSP00000483066.2:p.Val255=
ENST00000688158.2:n.1499T=
ENST00000688922.2:c.*594T= ENSP00000508742.2:n.*594T=
ENST00000700021.1:c.719T= ENSP00000514757.1:p.Val240=
ENST00000700022.1:c.*103T= ENSP00000514758.1:n.*103T=
ENST00000700023.1:n.1922T=
ENST00000700024.1:n.2156T=
ENST00000700025.1:n.1533T=
ENST00000700026.1:n.401T=
ENST00000700029.1:c.598T=
ENST00000706954.1:c.764T= ENSP00000516674.1:p.Val255=
ENST00000706955.1:c.*799T= ENSP00000516675.1:n.*799T=
ENST00000686459.1:c.*350T= ENSP00000508909.1:n.*350T=
ENST00000688158.1:c.*875T= ENSP00000509254.1:n.*875T=
ENST00000688308.1:c.764T= ENSP00000508752.1:p.Val255=
ENST00000688922.1:c.685T=
ENST00000693560.1:c.1283T= ENSP00000509861.1:p.Val428=
ENST00000371953.8:c.764T= MANE Select ENSP00000361021.3:p.Val255=
ENST00000371953.7:c.764T= ENSP00000361021.3:p.Val255=
ENST00000472832.2:c.191T= ENSP00000483066.1:p.Val64=
NM_000314.5:c.764T= NP_000305.3:p.Val255=
NM_000314.6:c.764T= NP_000305.3:p.Val255=
NM_001304717.2:c.1283T= NP_001291646.2:p.Val428=
NM_001304718.1:c.173T= NP_001291647.1:p.Val58=
XM_006717926.2:c.719T= XP_006717989.1:p.Val240=
XM_011539981.1:c.764T= XP_011538283.1:p.Val255=
XM_011539982.1:c.668T= XP_011538284.1:p.Val223=
XR_945791.1:n.1334T=
NM_000314.7:c.764T= NP_000305.3:p.Val255=
NM_001304717.5:c.1283T= NP_001291646.4:p.Val428=
NM_001304718.2:c.173T= NP_001291647.1:p.Val58=
NM_000314.8:c.764T= MANE Select NP_000305.3:p.Val255=