Canonical Allele Identifier: CA1926188593
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957974T= , CM000672.2:g.87957974T= GRCh38
NC_000010.10:g.89717731T= , CM000672.1:g.89717731T= GRCh37
NC_000010.9:g.89707711T= NCBI36
NG_007466.2:g.99536T= , LRG_311:g.99536T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.756T= ENSP00000514759.2:p.Asp252=
ENST00000710265.1:c.756T= ENSP00000518161.1:p.Asp252=
ENST00000472832.3:c.756T= ENSP00000483066.2:p.Asp252=
ENST00000688158.2:n.1491T=
ENST00000688922.2:c.*586T= ENSP00000508742.2:n.*586T=
ENST00000700021.1:c.711T= ENSP00000514757.1:p.Asp237=
ENST00000700022.1:c.*95T= ENSP00000514758.1:n.*95T=
ENST00000700023.1:n.1914T=
ENST00000700024.1:n.2148T=
ENST00000700025.1:n.1525T=
ENST00000700026.1:n.393T=
ENST00000700029.1:c.590T=
ENST00000706954.1:c.756T= ENSP00000516674.1:p.Asp252=
ENST00000706955.1:c.*791T= ENSP00000516675.1:n.*791T=
ENST00000686459.1:c.*342T= ENSP00000508909.1:n.*342T=
ENST00000688158.1:c.*867T= ENSP00000509254.1:n.*867T=
ENST00000688308.1:c.756T= ENSP00000508752.1:p.Asp252=
ENST00000688922.1:c.677T=
ENST00000693560.1:c.1275T= ENSP00000509861.1:p.Asp425=
ENST00000371953.8:c.756T= MANE Select ENSP00000361021.3:p.Asp252=
ENST00000371953.7:c.756T= ENSP00000361021.3:p.Asp252=
ENST00000472832.2:c.183T= ENSP00000483066.1:p.Asp61=
NM_000314.5:c.756T= NP_000305.3:p.Asp252=
NM_000314.6:c.756T= NP_000305.3:p.Asp252=
NM_001304717.2:c.1275T= NP_001291646.2:p.Asp425=
NM_001304718.1:c.165T= NP_001291647.1:p.Asp55=
XM_006717926.2:c.711T= XP_006717989.1:p.Asp237=
XM_011539981.1:c.756T= XP_011538283.1:p.Asp252=
XM_011539982.1:c.660T= XP_011538284.1:p.Asp220=
XR_945791.1:n.1326T=
NM_000314.7:c.756T= NP_000305.3:p.Asp252=
NM_001304717.5:c.1275T= NP_001291646.4:p.Asp425=
NM_001304718.2:c.165T= NP_001291647.1:p.Asp55=
NM_000314.8:c.756T= MANE Select NP_000305.3:p.Asp252=