Canonical Allele Identifier: CA000286
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 140777
dbSNP Id: rs587781273

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965338A>G , CM000672.2:g.87965338A>G GRCh38
NC_000010.10:g.89725095A>G , CM000672.1:g.89725095A>G GRCh37
NC_000010.9:g.89715075A>G NCBI36
NG_007466.2:g.106900A>G , LRG_311:g.106900A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1171A>G ENSP00000514759.2:p.Ser391Gly
ENST00000710265.1:c.*107A>G ENSP00000518161.1:n.*107A>G
ENST00000688158.2:n.1813A>G
ENST00000688922.2:c.*908A>G ENSP00000508742.2:n.*908A>G
ENST00000700021.1:c.1033A>G ENSP00000514757.1:p.Ser345Gly
ENST00000700022.1:c.*417A>G ENSP00000514758.1:n.*417A>G
ENST00000700023.1:n.2236A>G
ENST00000700024.1:n.2470A>G
ENST00000706954.1:c.1078A>G ENSP00000516674.1:p.Ser360Gly
ENST00000706955.1:c.*1113A>G ENSP00000516675.1:n.*1113A>G
ENST00000686459.1:c.*664A>G ENSP00000508909.1:n.*664A>G
ENST00000688158.1:c.*1189A>G ENSP00000509254.1:n.*1189A>G
ENST00000688308.1:c.1078A>G ENSP00000508752.1:p.Ser360Gly
ENST00000688922.1:c.999A>G
ENST00000693560.1:c.1597A>G ENSP00000509861.1:p.Ser533Gly
ENST00000371953.8:c.1078A>G MANE Select ENSP00000361021.3:p.Ser360Gly
ENST00000371953.7:c.1078A>G ENSP00000361021.3:p.Ser360Gly
NM_000314.5:c.1078A>G NP_000305.3:p.Ser360Gly
NM_000314.6:c.1078A>G NP_000305.3:p.Ser360Gly
NM_001304717.2:c.1597A>G NP_001291646.2:p.Ser533Gly
NM_001304718.1:c.487A>G NP_001291647.1:p.Ser163Gly
XM_006717926.2:c.1033A>G XP_006717989.1:p.Ser345Gly
XM_011539982.1:c.982A>G XP_011538284.1:p.Ser328Gly
XR_945791.1:n.1648A>G
NM_000314.7:c.1078A>G NP_000305.3:p.Ser360Gly
NM_001304717.5:c.1597A>G NP_001291646.4:p.Ser533Gly
NM_001304718.2:c.487A>G NP_001291647.1:p.Ser163Gly
NM_000314.8:c.1078A>G MANE Select NP_000305.3:p.Ser360Gly