Canonical Allele Identifier: CA1926188649
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958044G= , CM000672.2:g.87958044G= GRCh38
NC_000010.10:g.89717801G= , CM000672.1:g.89717801G= GRCh37
NC_000010.9:g.89707781G= NCBI36
NG_007466.2:g.99606G= , LRG_311:g.99606G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.801+25G= ENSP00000514759.2:n.801+25G=
ENST00000710265.1:c.801+25G= ENSP00000518161.1:n.801+25G=
ENST00000472832.3:c.801+25G= ENSP00000483066.2:n.801+25G=
ENST00000688158.2:n.1536+25G=
ENST00000688922.2:c.*631+25G= ENSP00000508742.2:n.*631+25G=
ENST00000700021.1:c.756+25G= ENSP00000514757.1:n.756+25G=
ENST00000700022.1:c.*140+25G= ENSP00000514758.1:n.*140+25G=
ENST00000700023.1:n.1959+25G=
ENST00000700024.1:n.2193+25G=
ENST00000700025.1:n.1570+25G=
ENST00000700026.1:n.438+25G=
ENST00000700029.1:c.635+25G=
ENST00000706954.1:c.801+25G= ENSP00000516674.1:n.801+25G=
ENST00000706955.1:c.*836+25G= ENSP00000516675.1:n.*836+25G=
ENST00000686459.1:c.*387+25G= ENSP00000508909.1:n.*387+25G=
ENST00000688158.1:c.*912+25G= ENSP00000509254.1:n.*912+25G=
ENST00000688308.1:c.801+25G= ENSP00000508752.1:n.801+25G=
ENST00000688922.1:c.722+25G=
ENST00000693560.1:c.1320+25G= ENSP00000509861.1:n.1320+25G=
ENST00000371953.8:c.801+25G= MANE Select ENSP00000361021.3:n.801+25G=
ENST00000371953.7:c.801+25G= ENSP00000361021.3:n.801+25G=
ENST00000472832.2:c.228+25G= ENSP00000483066.1:n.228+25G=
NM_000314.5:c.801+25G= NP_000305.3:n.801+25G=
NM_000314.6:c.801+25G= NP_000305.3:n.801+25G=
NM_001304717.2:c.1320+25G= NP_001291646.2:n.1320+25G=
NM_001304718.1:c.210+25G= NP_001291647.1:n.210+25G=
XM_006717926.2:c.756+25G= XP_006717989.1:n.756+25G=
XM_011539981.1:c.801+25G= XP_011538283.1:n.801+25G=
XM_011539982.1:c.705+25G= XP_011538284.1:n.705+25G=
XR_945791.1:n.1371+25G=
NM_000314.7:c.801+25G= NP_000305.3:n.801+25G=
NM_001304717.5:c.1320+25G= NP_001291646.4:n.1320+25G=
NM_001304718.2:c.210+25G= NP_001291647.1:n.210+25G=
NM_000314.8:c.801+25G= MANE Select NP_000305.3:n.801+25G=