Canonical Allele Identifier: CA377482203
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933090T>A , CM000672.2:g.87933090T>A GRCh38
NC_000010.10:g.89692847T>A , CM000672.1:g.89692847T>A GRCh37
NC_000010.9:g.89682827T>A NCBI36
NG_007466.2:g.74652T>A , LRG_311:g.74652T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.331T>A ENSP00000514759.2:p.Trp111Arg
ENST00000710265.1:c.331T>A ENSP00000518161.1:p.Trp111Arg
ENST00000472832.3:c.331T>A ENSP00000483066.2:p.Trp111Arg
ENST00000688158.2:n.1066T>A
ENST00000688922.2:c.*161T>A ENSP00000508742.2:n.*161T>A
ENST00000700021.1:c.286T>A ENSP00000514757.1:p.Trp96Arg
ENST00000700022.1:c.331T>A ENSP00000514758.1:p.Trp111Arg
ENST00000700029.1:c.165T>A
ENST00000706954.1:c.331T>A ENSP00000516674.1:p.Trp111Arg
ENST00000706955.1:c.*366T>A ENSP00000516675.1:n.*366T>A
ENST00000686459.1:c.331T>A ENSP00000508909.1:p.Trp111Arg
ENST00000688158.1:c.*442T>A ENSP00000509254.1:n.*442T>A
ENST00000688308.1:c.331T>A ENSP00000508752.1:p.Trp111Arg
ENST00000688922.1:c.252T>A
ENST00000693560.1:c.850T>A ENSP00000509861.1:p.Trp284Arg
ENST00000371953.8:c.331T>A MANE Select ENSP00000361021.3:p.Trp111Arg
ENST00000371953.7:c.331T>A ENSP00000361021.3:p.Trp111Arg
ENST00000498703.1:n.157T>A
ENST00000610634.1:c.229T>A ENSP00000477517.1:p.Trp77Arg
NM_000314.5:c.331T>A NP_000305.3:p.Trp111Arg
NM_000314.6:c.331T>A NP_000305.3:p.Trp111Arg
NM_001304717.2:c.850T>A NP_001291646.2:p.Trp284Arg
NM_001304718.1:c.-420T>A NP_001291647.1:n.-420T>A
XM_006717926.2:c.286T>A XP_006717989.1:p.Trp96Arg
XM_011539981.1:c.331T>A XP_011538283.1:p.Trp111Arg
XM_011539982.1:c.235T>A XP_011538284.1:p.Trp79Arg
XR_945789.1:n.1043T>A
XR_945790.1:n.1043T>A
XR_945791.1:n.1043T>A
NM_000314.7:c.331T>A NP_000305.3:p.Trp111Arg
NM_001304717.5:c.850T>A NP_001291646.4:p.Trp284Arg
NM_001304718.2:c.-420T>A NP_001291647.1:n.-420T>A
NM_000314.8:c.331T>A MANE Select NP_000305.3:p.Trp111Arg