Canonical Allele Identifier: CA1926188588
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957970G= , CM000672.2:g.87957970G= GRCh38
NC_000010.10:g.89717727G= , CM000672.1:g.89717727G= GRCh37
NC_000010.9:g.89707707G= NCBI36
NG_007466.2:g.99532G= , LRG_311:g.99532G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.752G= ENSP00000514759.2:p.Gly251=
ENST00000710265.1:c.752G= ENSP00000518161.1:p.Gly251=
ENST00000472832.3:c.752G= ENSP00000483066.2:p.Gly251=
ENST00000688158.2:n.1487G=
ENST00000688922.2:c.*582G= ENSP00000508742.2:n.*582G=
ENST00000700021.1:c.707G= ENSP00000514757.1:p.Gly236=
ENST00000700022.1:c.*91G= ENSP00000514758.1:n.*91G=
ENST00000700023.1:n.1910G=
ENST00000700024.1:n.2144G=
ENST00000700025.1:n.1521G=
ENST00000700026.1:n.389G=
ENST00000700029.1:c.586G=
ENST00000706954.1:c.752G= ENSP00000516674.1:p.Gly251=
ENST00000706955.1:c.*787G= ENSP00000516675.1:n.*787G=
ENST00000686459.1:c.*338G= ENSP00000508909.1:n.*338G=
ENST00000688158.1:c.*863G= ENSP00000509254.1:n.*863G=
ENST00000688308.1:c.752G= ENSP00000508752.1:p.Gly251=
ENST00000688922.1:c.673G=
ENST00000693560.1:c.1271G= ENSP00000509861.1:p.Gly424=
ENST00000371953.8:c.752G= MANE Select ENSP00000361021.3:p.Gly251=
ENST00000371953.7:c.752G= ENSP00000361021.3:p.Gly251=
ENST00000472832.2:c.179G= ENSP00000483066.1:p.Gly60=
NM_000314.5:c.752G= NP_000305.3:p.Gly251=
NM_000314.6:c.752G= NP_000305.3:p.Gly251=
NM_001304717.2:c.1271G= NP_001291646.2:p.Gly424=
NM_001304718.1:c.161G= NP_001291647.1:p.Gly54=
XM_006717926.2:c.707G= XP_006717989.1:p.Gly236=
XM_011539981.1:c.752G= XP_011538283.1:p.Gly251=
XM_011539982.1:c.656G= XP_011538284.1:p.Gly219=
XR_945791.1:n.1322G=
NM_000314.7:c.752G= NP_000305.3:p.Gly251=
NM_001304717.5:c.1271G= NP_001291646.4:p.Gly424=
NM_001304718.2:c.161G= NP_001291647.1:p.Gly54=
NM_000314.8:c.752G= MANE Select NP_000305.3:p.Gly251=