Canonical Allele Identifier: CA377485680
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960965A>T , CM000672.2:g.87960965A>T GRCh38
NC_000010.10:g.89720722A>T , CM000672.1:g.89720722A>T GRCh37
NC_000010.9:g.89710702A>T NCBI36
NG_007466.2:g.102527A>T , LRG_311:g.102527A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.966A>T ENSP00000514759.2:p.Glu322Asp
ENST00000710265.1:c.873A>T ENSP00000518161.1:p.Glu291Asp
ENST00000472832.3:c.873A>T ENSP00000483066.2:p.Glu291Asp
ENST00000688158.2:n.1608A>T
ENST00000688922.2:c.*703A>T ENSP00000508742.2:n.*703A>T
ENST00000700021.1:c.828A>T ENSP00000514757.1:p.Glu276Asp
ENST00000700022.1:c.*212A>T ENSP00000514758.1:n.*212A>T
ENST00000700023.1:n.2031A>T
ENST00000700024.1:n.2265A>T
ENST00000700025.1:n.1642A>T
ENST00000700026.1:n.510A>T
ENST00000700029.1:c.800A>T
ENST00000706954.1:c.873A>T ENSP00000516674.1:p.Glu291Asp
ENST00000706955.1:c.*908A>T ENSP00000516675.1:n.*908A>T
ENST00000686459.1:c.*459A>T ENSP00000508909.1:n.*459A>T
ENST00000688158.1:c.*984A>T ENSP00000509254.1:n.*984A>T
ENST00000688308.1:c.873A>T ENSP00000508752.1:p.Glu291Asp
ENST00000688922.1:c.794A>T
ENST00000693560.1:c.1392A>T ENSP00000509861.1:p.Glu464Asp
ENST00000371953.8:c.873A>T MANE Select ENSP00000361021.3:p.Glu291Asp
ENST00000371953.7:c.873A>T ENSP00000361021.3:p.Glu291Asp
ENST00000472832.2:c.300A>T ENSP00000483066.1:p.Glu100Asp
NM_000314.5:c.873A>T NP_000305.3:p.Glu291Asp
NM_000314.6:c.873A>T NP_000305.3:p.Glu291Asp
NM_001304717.2:c.1392A>T NP_001291646.2:p.Glu464Asp
NM_001304718.1:c.282A>T NP_001291647.1:p.Glu94Asp
XM_006717926.2:c.828A>T XP_006717989.1:p.Glu276Asp
XM_011539981.1:c.873A>T XP_011538283.1:p.Glu291Asp
XM_011539982.1:c.777A>T XP_011538284.1:p.Glu259Asp
XR_945791.1:n.1443A>T
NM_000314.7:c.873A>T NP_000305.3:p.Glu291Asp
NM_001304717.5:c.1392A>T NP_001291646.4:p.Glu464Asp
NM_001304718.2:c.282A>T NP_001291647.1:p.Glu94Asp
NM_000314.8:c.873A>T MANE Select NP_000305.3:p.Glu291Asp