Canonical Allele Identifier: CA377485714
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs143335584

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960974T>A , CM000672.2:g.87960974T>A GRCh38
NC_000010.10:g.89720731T>A , CM000672.1:g.89720731T>A GRCh37
NC_000010.9:g.89710711T>A NCBI36
NG_007466.2:g.102536T>A , LRG_311:g.102536T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.975T>A ENSP00000514759.2:p.Ser325Arg
ENST00000710265.1:c.882T>A ENSP00000518161.1:p.Ser294Arg
ENST00000472832.3:c.882T>A ENSP00000483066.2:p.Ser294Arg
ENST00000688158.2:n.1617T>A
ENST00000688922.2:c.*712T>A ENSP00000508742.2:n.*712T>A
ENST00000700021.1:c.837T>A ENSP00000514757.1:p.Ser279Arg
ENST00000700022.1:c.*221T>A ENSP00000514758.1:n.*221T>A
ENST00000700023.1:n.2040T>A
ENST00000700024.1:n.2274T>A
ENST00000700025.1:n.1651T>A
ENST00000700026.1:n.519T>A
ENST00000706954.1:c.882T>A ENSP00000516674.1:p.Ser294Arg
ENST00000706955.1:c.*917T>A ENSP00000516675.1:n.*917T>A
ENST00000686459.1:c.*468T>A ENSP00000508909.1:n.*468T>A
ENST00000688158.1:c.*993T>A ENSP00000509254.1:n.*993T>A
ENST00000688308.1:c.882T>A ENSP00000508752.1:p.Ser294Arg
ENST00000688922.1:c.803T>A
ENST00000693560.1:c.1401T>A ENSP00000509861.1:p.Ser467Arg
ENST00000371953.8:c.882T>A MANE Select ENSP00000361021.3:p.Ser294Arg
ENST00000371953.7:c.882T>A ENSP00000361021.3:p.Ser294Arg
ENST00000472832.2:c.309T>A ENSP00000483066.1:p.Ser103Arg
NM_000314.5:c.882T>A NP_000305.3:p.Ser294Arg
NM_000314.6:c.882T>A NP_000305.3:p.Ser294Arg
NM_001304717.2:c.1401T>A NP_001291646.2:p.Ser467Arg
NM_001304718.1:c.291T>A NP_001291647.1:p.Ser97Arg
XM_006717926.2:c.837T>A XP_006717989.1:p.Ser279Arg
XM_011539981.1:c.882T>A XP_011538283.1:p.Ser294Arg
XM_011539982.1:c.786T>A XP_011538284.1:p.Ser262Arg
XR_945791.1:n.1452T>A
NM_000314.7:c.882T>A NP_000305.3:p.Ser294Arg
NM_001304717.5:c.1401T>A NP_001291646.4:p.Ser467Arg
NM_001304718.2:c.291T>A NP_001291647.1:p.Ser97Arg
NM_000314.8:c.882T>A MANE Select NP_000305.3:p.Ser294Arg