Canonical Allele Identifier: CA2610045342
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894178A>T , CM000672.2:g.87894178A>T GRCh38
NC_000010.10:g.89653935A>T , CM000672.1:g.89653935A>T GRCh37
NC_000010.9:g.89643915A>T NCBI36
NG_007466.2:g.35740A>T , LRG_311:g.35740A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.164+69A>T ENSP00000514759.2:n.164+69A>T
ENST00000710265.1:c.164+69A>T ENSP00000518161.1:n.164+69A>T
ENST00000472832.3:c.164+69A>T ENSP00000483066.2:n.164+69A>T
ENST00000688158.2:n.899+13740A>T
ENST00000688922.2:c.164+69A>T ENSP00000508742.2:n.164+69A>T
ENST00000700021.1:c.164+69A>T ENSP00000514757.1:n.164+69A>T
ENST00000700022.1:c.164+69A>T ENSP00000514758.1:n.164+69A>T
ENST00000706954.1:c.164+69A>T ENSP00000516674.1:n.164+69A>T
ENST00000706955.1:c.*199+69A>T ENSP00000516675.1:n.*199+69A>T
ENST00000686459.1:c.164+69A>T ENSP00000508909.1:n.164+69A>T
ENST00000688158.1:c.*275+13740A>T ENSP00000509254.1:n.*275+13740A>T
ENST00000688308.1:c.164+69A>T ENSP00000508752.1:n.164+69A>T
ENST00000688922.1:c.33+69A>T
ENST00000693560.1:c.683+69A>T ENSP00000509861.1:n.683+69A>T
ENST00000371953.8:c.164+69A>T MANE Select ENSP00000361021.3:n.164+69A>T
ENST00000371953.7:c.164+69A>T ENSP00000361021.3:n.164+69A>T
ENST00000462694.1:n.235A>T
ENST00000610634.1:c.62+69A>T ENSP00000477517.1:n.62+69A>T
NM_000314.5:c.164+69A>T NP_000305.3:n.164+69A>T
NM_000314.6:c.164+69A>T NP_000305.3:n.164+69A>T
NM_001304717.2:c.683+69A>T NP_001291646.2:n.683+69A>T
NM_001304718.1:c.-542+69A>T NP_001291647.1:n.-542+69A>T
XM_006717926.2:c.164+69A>T XP_006717989.1:n.164+69A>T
XM_011539981.1:c.164+69A>T XP_011538283.1:n.164+69A>T
XM_011539982.1:c.68+13740A>T XP_011538284.1:n.68+13740A>T
XR_945789.1:n.876+69A>T
XR_945790.1:n.876+69A>T
XR_945791.1:n.876+69A>T
NM_000314.7:c.164+69A>T NP_000305.3:n.164+69A>T
NM_001304717.5:c.683+69A>T NP_001291646.4:n.683+69A>T
NM_001304718.2:c.-542+69A>T NP_001291647.1:n.-542+69A>T
NM_000314.8:c.164+69A>T MANE Select NP_000305.3:n.164+69A>T