Canonical Allele Identifier: CA1926188571
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957953G= , CM000672.2:g.87957953G= GRCh38
NC_000010.10:g.89717710G= , CM000672.1:g.89717710G= GRCh37
NC_000010.9:g.89707690G= NCBI36
NG_007466.2:g.99515G= , LRG_311:g.99515G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.735G= ENSP00000514759.2:p.Gln245=
ENST00000710265.1:c.735G= ENSP00000518161.1:p.Gln245=
ENST00000472832.3:c.735G= ENSP00000483066.2:p.Gln245=
ENST00000688158.2:n.1470G=
ENST00000688922.2:c.*565G= ENSP00000508742.2:n.*565G=
ENST00000700021.1:c.690G= ENSP00000514757.1:p.Gln230=
ENST00000700022.1:c.*74G= ENSP00000514758.1:n.*74G=
ENST00000700023.1:n.1893G=
ENST00000700024.1:n.2127G=
ENST00000700025.1:n.1504G=
ENST00000700026.1:n.372G=
ENST00000700029.1:c.569G=
ENST00000706954.1:c.735G= ENSP00000516674.1:p.Gln245=
ENST00000706955.1:c.*770G= ENSP00000516675.1:n.*770G=
ENST00000686459.1:c.*321G= ENSP00000508909.1:n.*321G=
ENST00000688158.1:c.*846G= ENSP00000509254.1:n.*846G=
ENST00000688308.1:c.735G= ENSP00000508752.1:p.Gln245=
ENST00000688922.1:c.656G=
ENST00000693560.1:c.1254G= ENSP00000509861.1:p.Gln418=
ENST00000371953.8:c.735G= MANE Select ENSP00000361021.3:p.Gln245=
ENST00000371953.7:c.735G= ENSP00000361021.3:p.Gln245=
ENST00000472832.2:c.162G= ENSP00000483066.1:p.Gln54=
NM_000314.5:c.735G= NP_000305.3:p.Gln245=
NM_000314.6:c.735G= NP_000305.3:p.Gln245=
NM_001304717.2:c.1254G= NP_001291646.2:p.Gln418=
NM_001304718.1:c.144G= NP_001291647.1:p.Gln48=
XM_006717926.2:c.690G= XP_006717989.1:p.Gln230=
XM_011539981.1:c.735G= XP_011538283.1:p.Gln245=
XM_011539982.1:c.639G= XP_011538284.1:p.Gln213=
XR_945791.1:n.1305G=
NM_000314.7:c.735G= NP_000305.3:p.Gln245=
NM_001304717.5:c.1254G= NP_001291646.4:p.Gln418=
NM_001304718.2:c.144G= NP_001291647.1:p.Gln48=
NM_000314.8:c.735G= MANE Select NP_000305.3:p.Gln245=