Canonical Allele Identifier: CA1926188610
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957998A= , CM000672.2:g.87957998A= GRCh38
NC_000010.10:g.89717755A= , CM000672.1:g.89717755A= GRCh37
NC_000010.9:g.89707735A= NCBI36
NG_007466.2:g.99560A= , LRG_311:g.99560A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.780A= ENSP00000514759.2:p.Lys260=
ENST00000710265.1:c.780A= ENSP00000518161.1:p.Lys260=
ENST00000472832.3:c.780A= ENSP00000483066.2:p.Lys260=
ENST00000688158.2:n.1515A=
ENST00000688922.2:c.*610A= ENSP00000508742.2:n.*610A=
ENST00000700021.1:c.735A= ENSP00000514757.1:p.Lys245=
ENST00000700022.1:c.*119A= ENSP00000514758.1:n.*119A=
ENST00000700023.1:n.1938A=
ENST00000700024.1:n.2172A=
ENST00000700025.1:n.1549A=
ENST00000700026.1:n.417A=
ENST00000700029.1:c.614A=
ENST00000706954.1:c.780A= ENSP00000516674.1:p.Lys260=
ENST00000706955.1:c.*815A= ENSP00000516675.1:n.*815A=
ENST00000686459.1:c.*366A= ENSP00000508909.1:n.*366A=
ENST00000688158.1:c.*891A= ENSP00000509254.1:n.*891A=
ENST00000688308.1:c.780A= ENSP00000508752.1:p.Lys260=
ENST00000688922.1:c.701A=
ENST00000693560.1:c.1299A= ENSP00000509861.1:p.Lys433=
ENST00000371953.8:c.780A= MANE Select ENSP00000361021.3:p.Lys260=
ENST00000371953.7:c.780A= ENSP00000361021.3:p.Lys260=
ENST00000472832.2:c.207A= ENSP00000483066.1:p.Lys69=
NM_000314.5:c.780A= NP_000305.3:p.Lys260=
NM_000314.6:c.780A= NP_000305.3:p.Lys260=
NM_001304717.2:c.1299A= NP_001291646.2:p.Lys433=
NM_001304718.1:c.189A= NP_001291647.1:p.Lys63=
XM_006717926.2:c.735A= XP_006717989.1:p.Lys245=
XM_011539981.1:c.780A= XP_011538283.1:p.Lys260=
XM_011539982.1:c.684A= XP_011538284.1:p.Lys228=
XR_945791.1:n.1350A=
NM_000314.7:c.780A= NP_000305.3:p.Lys260=
NM_001304717.5:c.1299A= NP_001291646.4:p.Lys433=
NM_001304718.2:c.189A= NP_001291647.1:p.Lys63=
NM_000314.8:c.780A= MANE Select NP_000305.3:p.Lys260=