Canonical Allele Identifier: CA377484873
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132276903

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957912A>T , CM000672.2:g.87957912A>T GRCh38
NC_000010.10:g.89717669A>T , CM000672.1:g.89717669A>T GRCh37
NC_000010.9:g.89707649A>T NCBI36
NG_007466.2:g.99474A>T , LRG_311:g.99474A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.694A>T ENSP00000514759.2:p.Thr232Ser
ENST00000710265.1:c.694A>T ENSP00000518161.1:p.Thr232Ser
ENST00000472832.3:c.694A>T ENSP00000483066.2:p.Thr232Ser
ENST00000688158.2:n.1429A>T
ENST00000688922.2:c.*524A>T ENSP00000508742.2:n.*524A>T
ENST00000700021.1:c.649A>T ENSP00000514757.1:p.Thr217Ser
ENST00000700022.1:c.*33A>T ENSP00000514758.1:n.*33A>T
ENST00000700023.1:n.1852A>T
ENST00000700024.1:n.2086A>T
ENST00000700025.1:n.1463A>T
ENST00000700026.1:n.331A>T
ENST00000700029.1:c.528A>T
ENST00000706954.1:c.694A>T ENSP00000516674.1:p.Thr232Ser
ENST00000706955.1:c.*729A>T ENSP00000516675.1:n.*729A>T
ENST00000686459.1:c.*280A>T ENSP00000508909.1:n.*280A>T
ENST00000688158.1:c.*805A>T ENSP00000509254.1:n.*805A>T
ENST00000688308.1:c.694A>T ENSP00000508752.1:p.Thr232Ser
ENST00000688922.1:c.615A>T
ENST00000693560.1:c.1213A>T ENSP00000509861.1:p.Thr405Ser
ENST00000371953.8:c.694A>T MANE Select ENSP00000361021.3:p.Thr232Ser
ENST00000371953.7:c.694A>T ENSP00000361021.3:p.Thr232Ser
ENST00000472832.2:c.121A>T ENSP00000483066.1:p.Thr41Ser
NM_000314.5:c.694A>T NP_000305.3:p.Thr232Ser
NM_000314.6:c.694A>T NP_000305.3:p.Thr232Ser
NM_001304717.2:c.1213A>T NP_001291646.2:p.Thr405Ser
NM_001304718.1:c.103A>T NP_001291647.1:p.Thr35Ser
XM_006717926.2:c.649A>T XP_006717989.1:p.Thr217Ser
XM_011539981.1:c.694A>T XP_011538283.1:p.Thr232Ser
XM_011539982.1:c.598A>T XP_011538284.1:p.Thr200Ser
XR_945791.1:n.1264A>T
NM_000314.7:c.694A>T NP_000305.3:p.Thr232Ser
NM_001304717.5:c.1213A>T NP_001291646.4:p.Thr405Ser
NM_001304718.2:c.103A>T NP_001291647.1:p.Thr35Ser
NM_000314.8:c.694A>T MANE Select NP_000305.3:p.Thr232Ser