Canonical Allele Identifier: CA2610047784
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960891_87960892insTTTTGGGAAAAAAAAAATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000672.2:g.87960891_87960892insTTTTGGGAAAAAAAAAATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000010.10:g.89720648_89720649insTTTTGGGAAAAAAAAAATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000672.1:g.89720648_89720649insTTTTGGGAAAAAAAAAATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000010.9:g.89710628_89710629insTTTTGGGAAAAAAAAAATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_007466.2:g.102453_102454insTTTTGGGAAAAAAAAAATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_311:g.102453_102454insTTTTGGGAAAAAAAAAATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

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