Canonical Allele Identifier: CA377485488
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960912T>A , CM000672.2:g.87960912T>A GRCh38
NC_000010.10:g.89720669T>A , CM000672.1:g.89720669T>A GRCh37
NC_000010.9:g.89710649T>A NCBI36
NG_007466.2:g.102474T>A , LRG_311:g.102474T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.913T>A ENSP00000514759.2:p.Trp305Arg
ENST00000710265.1:c.820T>A ENSP00000518161.1:p.Trp274Arg
ENST00000472832.3:c.820T>A ENSP00000483066.2:p.Trp274Arg
ENST00000688158.2:n.1555T>A
ENST00000688922.2:c.*650T>A ENSP00000508742.2:n.*650T>A
ENST00000700021.1:c.775T>A ENSP00000514757.1:p.Trp259Arg
ENST00000700022.1:c.*159T>A ENSP00000514758.1:n.*159T>A
ENST00000700023.1:n.1978T>A
ENST00000700024.1:n.2212T>A
ENST00000700025.1:n.1589T>A
ENST00000700026.1:n.457T>A
ENST00000700029.1:c.747T>A
ENST00000706954.1:c.820T>A ENSP00000516674.1:p.Trp274Arg
ENST00000706955.1:c.*855T>A ENSP00000516675.1:n.*855T>A
ENST00000686459.1:c.*406T>A ENSP00000508909.1:n.*406T>A
ENST00000688158.1:c.*931T>A ENSP00000509254.1:n.*931T>A
ENST00000688308.1:c.820T>A ENSP00000508752.1:p.Trp274Arg
ENST00000688922.1:c.741T>A
ENST00000693560.1:c.1339T>A ENSP00000509861.1:p.Trp447Arg
ENST00000371953.8:c.820T>A MANE Select ENSP00000361021.3:p.Trp274Arg
ENST00000371953.7:c.820T>A ENSP00000361021.3:p.Trp274Arg
ENST00000472832.2:c.247T>A ENSP00000483066.1:p.Trp83Arg
NM_000314.5:c.820T>A NP_000305.3:p.Trp274Arg
NM_000314.6:c.820T>A NP_000305.3:p.Trp274Arg
NM_001304717.2:c.1339T>A NP_001291646.2:p.Trp447Arg
NM_001304718.1:c.229T>A NP_001291647.1:p.Trp77Arg
XM_006717926.2:c.775T>A XP_006717989.1:p.Trp259Arg
XM_011539981.1:c.820T>A XP_011538283.1:p.Trp274Arg
XM_011539982.1:c.724T>A XP_011538284.1:p.Trp242Arg
XR_945791.1:n.1390T>A
NM_000314.7:c.820T>A NP_000305.3:p.Trp274Arg
NM_001304717.5:c.1339T>A NP_001291646.4:p.Trp447Arg
NM_001304718.2:c.229T>A NP_001291647.1:p.Trp77Arg
NM_000314.8:c.820T>A MANE Select NP_000305.3:p.Trp274Arg