Canonical Allele Identifier: CA1926172948
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965111C= , CM000672.2:g.87965111C= GRCh38
NC_000010.10:g.89724868C= , CM000672.1:g.89724868C= GRCh37
NC_000010.9:g.89714848C= NCBI36
NG_007466.2:g.106673C= , LRG_311:g.106673C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1120-176C= ENSP00000514759.2:n.1120-176C=
ENST00000710265.1:c.*56-176C= ENSP00000518161.1:n.*56-176C=
ENST00000688158.2:n.1762-176C=
ENST00000688922.2:c.*857-176C= ENSP00000508742.2:n.*857-176C=
ENST00000700021.1:c.982-176C= ENSP00000514757.1:n.982-176C=
ENST00000700022.1:c.*366-176C= ENSP00000514758.1:n.*366-176C=
ENST00000700023.1:n.2185-176C=
ENST00000700024.1:n.2419-176C=
ENST00000706954.1:c.1027-176C= ENSP00000516674.1:n.1027-176C=
ENST00000706955.1:c.*1062-176C= ENSP00000516675.1:n.*1062-176C=
ENST00000686459.1:c.*613-176C= ENSP00000508909.1:n.*613-176C=
ENST00000688158.1:c.*1138-176C= ENSP00000509254.1:n.*1138-176C=
ENST00000688308.1:c.1027-176C= ENSP00000508752.1:n.1027-176C=
ENST00000688922.1:c.948-176C=
ENST00000693560.1:c.1546-176C= ENSP00000509861.1:n.1546-176C=
ENST00000371953.8:c.1027-176C= MANE Select ENSP00000361021.3:n.1027-176C=
ENST00000371953.7:c.1027-176C= ENSP00000361021.3:n.1027-176C=
NM_000314.5:c.1027-176C= NP_000305.3:n.1027-176C=
NM_000314.6:c.1027-176C= NP_000305.3:n.1027-176C=
NM_001304717.2:c.1546-176C= NP_001291646.2:n.1546-176C=
NM_001304718.1:c.436-176C= NP_001291647.1:n.436-176C=
XM_006717926.2:c.982-176C= XP_006717989.1:n.982-176C=
XM_011539982.1:c.931-176C= XP_011538284.1:n.931-176C=
XR_945791.1:n.1597-176C=
NM_000314.7:c.1027-176C= NP_000305.3:n.1027-176C=
NM_001304717.5:c.1546-176C= NP_001291646.4:n.1546-176C=
NM_001304718.2:c.436-176C= NP_001291647.1:n.436-176C=
NM_000314.8:c.1027-176C= MANE Select NP_000305.3:n.1027-176C=