Canonical Allele Identifier: CA1926189883
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960847_87960850delinsAAAT , CM000672.2:g.87960847_87960850delinsAAAT GRCh38
NC_000010.10:g.89720604_89720607delinsAAAT , CM000672.1:g.89720604_89720607delinsAAAT GRCh37
NC_000010.9:g.89710584_89710587delinsAAAT NCBI36
NG_007466.2:g.102409_102412delinsAAAT , LRG_311:g.102409_102412delinsAAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.895-47_895-44delinsAAAT ENSP00000514759.2:n.895-47_895-44delinsAA...
ENST00000710265.1:c.802-47_802-44delinsAAAT ENSP00000518161.1:n.802-47_802-44delinsAA...
ENST00000472832.3:c.802-47_802-44delinsAAAT ENSP00000483066.2:n.802-47_802-44delinsAA...
ENST00000688158.2:n.1537-47_1537-44delinsAAAT
ENST00000688922.2:c.*632-47_*632-44delinsAAAT ENSP00000508742.2:n.*632-47_*632-44delins...
ENST00000700021.1:c.757-47_757-44delinsAAAT ENSP00000514757.1:n.757-47_757-44delinsAA...
ENST00000700022.1:c.*141-47_*141-44delinsAAAT ENSP00000514758.1:n.*141-47_*141-44delins...
ENST00000700023.1:n.1960-47_1960-44delinsAAAT
ENST00000700024.1:n.2194-47_2194-44delinsAAAT
ENST00000700025.1:n.1571-47_1571-44delinsAAAT
ENST00000700026.1:n.439-47_439-44delinsAAAT
ENST00000700029.1:c.729-47_729-44delinsAAAT
ENST00000706954.1:c.802-47_802-44delinsAAAT ENSP00000516674.1:n.802-47_802-44delinsAA...
ENST00000706955.1:c.*837-47_*837-44delinsAAAT ENSP00000516675.1:n.*837-47_*837-44delins...
ENST00000686459.1:c.*388-47_*388-44delinsAAAT ENSP00000508909.1:n.*388-47_*388-44delins...
ENST00000688158.1:c.*913-47_*913-44delinsAAAT ENSP00000509254.1:n.*913-47_*913-44delins...
ENST00000688308.1:c.802-47_802-44delinsAAAT ENSP00000508752.1:n.802-47_802-44delinsAA...
ENST00000688922.1:c.723-47_723-44delinsAAAT
ENST00000693560.1:c.1321-47_1321-44delinsAAAT ENSP00000509861.1:n.1321-47_1321-44delins...
ENST00000371953.8:c.802-47_802-44delinsAAAT MANE Select ENSP00000361021.3:n.802-47_802-44delinsAA...
ENST00000371953.7:c.802-47_802-44delinsAAAT ENSP00000361021.3:n.802-47_802-44delinsAA...
ENST00000472832.2:c.229-47_229-44delinsAAAT ENSP00000483066.1:n.229-47_229-44delinsAA...
NM_000314.5:c.802-47_802-44delinsAAAT NP_000305.3:n.802-47_802-44delinsAAAT
NM_000314.6:c.802-47_802-44delinsAAAT NP_000305.3:n.802-47_802-44delinsAAAT
NM_001304717.2:c.1321-47_1321-44delinsAAAT NP_001291646.2:n.1321-47_1321-44delinsAAA...
NM_001304718.1:c.211-47_211-44delinsAAAT NP_001291647.1:n.211-47_211-44delinsAAAT
XM_006717926.2:c.757-47_757-44delinsAAAT XP_006717989.1:n.757-47_757-44delinsAAAT
XM_011539981.1:c.802-47_802-44delinsAAAT XP_011538283.1:n.802-47_802-44delinsAAAT
XM_011539982.1:c.706-47_706-44delinsAAAT XP_011538284.1:n.706-47_706-44delinsAAAT
XR_945791.1:n.1372-47_1372-44delinsAAAT
NM_000314.7:c.802-47_802-44delinsAAAT NP_000305.3:n.802-47_802-44delinsAAAT
NM_001304717.5:c.1321-47_1321-44delinsAAAT NP_001291646.4:n.1321-47_1321-44delinsAAA...
NM_001304718.2:c.211-47_211-44delinsAAAT NP_001291647.1:n.211-47_211-44delinsAAAT
NM_000314.8:c.802-47_802-44delinsAAAT MANE Select NP_000305.3:n.802-47_802-44delinsAAAT