Canonical Allele Identifier: CA377487257
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965368A>G , CM000672.2:g.87965368A>G GRCh38
NC_000010.10:g.89725125A>G , CM000672.1:g.89725125A>G GRCh37
NC_000010.9:g.89715105A>G NCBI36
NG_007466.2:g.106930A>G , LRG_311:g.106930A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1201A>G ENSP00000514759.2:p.Ser401Gly
ENST00000710265.1:c.*137A>G ENSP00000518161.1:n.*137A>G
ENST00000688158.2:n.1843A>G
ENST00000688922.2:c.*938A>G ENSP00000508742.2:n.*938A>G
ENST00000700021.1:c.1063A>G ENSP00000514757.1:p.Ser355Gly
ENST00000700022.1:c.*447A>G ENSP00000514758.1:n.*447A>G
ENST00000700023.1:n.2266A>G
ENST00000700024.1:n.2500A>G
ENST00000706954.1:c.1108A>G ENSP00000516674.1:p.Ser370Gly
ENST00000706955.1:c.*1143A>G ENSP00000516675.1:n.*1143A>G
ENST00000686459.1:c.*694A>G ENSP00000508909.1:n.*694A>G
ENST00000688158.1:c.*1219A>G ENSP00000509254.1:n.*1219A>G
ENST00000688308.1:c.1108A>G ENSP00000508752.1:p.Ser370Gly
ENST00000688922.1:c.1029A>G
ENST00000693560.1:c.1627A>G ENSP00000509861.1:p.Ser543Gly
ENST00000371953.8:c.1108A>G MANE Select ENSP00000361021.3:p.Ser370Gly
ENST00000371953.7:c.1108A>G ENSP00000361021.3:p.Ser370Gly
NM_000314.5:c.1108A>G NP_000305.3:p.Ser370Gly
NM_000314.6:c.1108A>G NP_000305.3:p.Ser370Gly
NM_001304717.2:c.1627A>G NP_001291646.2:p.Ser543Gly
NM_001304718.1:c.517A>G NP_001291647.1:p.Ser173Gly
XM_006717926.2:c.1063A>G XP_006717989.1:p.Ser355Gly
XM_011539982.1:c.1012A>G XP_011538284.1:p.Ser338Gly
XR_945791.1:n.1678A>G
NM_000314.7:c.1108A>G NP_000305.3:p.Ser370Gly
NM_001304717.5:c.1627A>G NP_001291646.4:p.Ser543Gly
NM_001304718.2:c.517A>G NP_001291647.1:p.Ser173Gly
NM_000314.8:c.1108A>G MANE Select NP_000305.3:p.Ser370Gly