Canonical Allele Identifier: CA377485911
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132282896

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961028C>A , CM000672.2:g.87961028C>A GRCh38
NC_000010.10:g.89720785C>A , CM000672.1:g.89720785C>A GRCh37
NC_000010.9:g.89710765C>A NCBI36
NG_007466.2:g.102590C>A , LRG_311:g.102590C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1029C>A ENSP00000514759.2:p.Asp343Glu
ENST00000710265.1:c.936C>A ENSP00000518161.1:p.Asp312Glu
ENST00000472832.3:c.936C>A ENSP00000483066.2:p.Asp312Glu
ENST00000688158.2:n.1671C>A
ENST00000688922.2:c.*766C>A ENSP00000508742.2:n.*766C>A
ENST00000700021.1:c.891C>A ENSP00000514757.1:p.Asp297Glu
ENST00000700022.1:c.*275C>A ENSP00000514758.1:n.*275C>A
ENST00000700023.1:n.2094C>A
ENST00000700024.1:n.2328C>A
ENST00000700025.1:n.1705C>A
ENST00000700026.1:n.573C>A
ENST00000706954.1:c.936C>A ENSP00000516674.1:p.Asp312Glu
ENST00000706955.1:c.*971C>A ENSP00000516675.1:n.*971C>A
ENST00000686459.1:c.*522C>A ENSP00000508909.1:n.*522C>A
ENST00000688158.1:c.*1047C>A ENSP00000509254.1:n.*1047C>A
ENST00000688308.1:c.936C>A ENSP00000508752.1:p.Asp312Glu
ENST00000688922.1:c.857C>A
ENST00000693560.1:c.1455C>A ENSP00000509861.1:p.Asp485Glu
ENST00000371953.8:c.936C>A MANE Select ENSP00000361021.3:p.Asp312Glu
ENST00000371953.7:c.936C>A ENSP00000361021.3:p.Asp312Glu
ENST00000472832.2:c.363C>A ENSP00000483066.1:p.Asp121Glu
NM_000314.5:c.936C>A NP_000305.3:p.Asp312Glu
NM_000314.6:c.936C>A NP_000305.3:p.Asp312Glu
NM_001304717.2:c.1455C>A NP_001291646.2:p.Asp485Glu
NM_001304718.1:c.345C>A NP_001291647.1:p.Asp115Glu
XM_006717926.2:c.891C>A XP_006717989.1:p.Asp297Glu
XM_011539981.1:c.936C>A XP_011538283.1:p.Asp312Glu
XM_011539982.1:c.840C>A XP_011538284.1:p.Asp280Glu
XR_945791.1:n.1506C>A
NM_000314.7:c.936C>A NP_000305.3:p.Asp312Glu
NM_001304717.5:c.1455C>A NP_001291646.4:p.Asp485Glu
NM_001304718.2:c.345C>A NP_001291647.1:p.Asp115Glu
NM_000314.8:c.936C>A MANE Select NP_000305.3:p.Asp312Glu