Canonical Allele Identifier: CA377485802
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs876660906

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960998C>A , CM000672.2:g.87960998C>A GRCh38
NC_000010.10:g.89720755C>A , CM000672.1:g.89720755C>A GRCh37
NC_000010.9:g.89710735C>A NCBI36
NG_007466.2:g.102560C>A , LRG_311:g.102560C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.999C>A ENSP00000514759.2:p.Ser333Arg
ENST00000710265.1:c.906C>A ENSP00000518161.1:p.Ser302Arg
ENST00000472832.3:c.906C>A ENSP00000483066.2:p.Ser302Arg
ENST00000688158.2:n.1641C>A
ENST00000688922.2:c.*736C>A ENSP00000508742.2:n.*736C>A
ENST00000700021.1:c.861C>A ENSP00000514757.1:p.Ser287Arg
ENST00000700022.1:c.*245C>A ENSP00000514758.1:n.*245C>A
ENST00000700023.1:n.2064C>A
ENST00000700024.1:n.2298C>A
ENST00000700025.1:n.1675C>A
ENST00000700026.1:n.543C>A
ENST00000706954.1:c.906C>A ENSP00000516674.1:p.Ser302Arg
ENST00000706955.1:c.*941C>A ENSP00000516675.1:n.*941C>A
ENST00000686459.1:c.*492C>A ENSP00000508909.1:n.*492C>A
ENST00000688158.1:c.*1017C>A ENSP00000509254.1:n.*1017C>A
ENST00000688308.1:c.906C>A ENSP00000508752.1:p.Ser302Arg
ENST00000688922.1:c.827C>A
ENST00000693560.1:c.1425C>A ENSP00000509861.1:p.Ser475Arg
ENST00000371953.8:c.906C>A MANE Select ENSP00000361021.3:p.Ser302Arg
ENST00000371953.7:c.906C>A ENSP00000361021.3:p.Ser302Arg
ENST00000472832.2:c.333C>A ENSP00000483066.1:p.Ser111Arg
NM_000314.5:c.906C>A NP_000305.3:p.Ser302Arg
NM_000314.6:c.906C>A NP_000305.3:p.Ser302Arg
NM_001304717.2:c.1425C>A NP_001291646.2:p.Ser475Arg
NM_001304718.1:c.315C>A NP_001291647.1:p.Ser105Arg
XM_006717926.2:c.861C>A XP_006717989.1:p.Ser287Arg
XM_011539981.1:c.906C>A XP_011538283.1:p.Ser302Arg
XM_011539982.1:c.810C>A XP_011538284.1:p.Ser270Arg
XR_945791.1:n.1476C>A
NM_000314.7:c.906C>A NP_000305.3:p.Ser302Arg
NM_001304717.5:c.1425C>A NP_001291646.4:p.Ser475Arg
NM_001304718.2:c.315C>A NP_001291647.1:p.Ser105Arg
NM_000314.8:c.906C>A MANE Select NP_000305.3:p.Ser302Arg