Canonical Allele Identifier: CA930923726
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960704_87960705insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG , CM000672.2:g.87960704_87960705insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG GRCh38
NC_000010.10:g.89720461_89720462insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG , CM000672.1:g.89720461_89720462insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG GRCh37
NC_000010.9:g.89710441_89710442insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG NCBI36
NG_007466.2:g.102266_102267insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG , LRG_311:g.102266_102267insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.895-190_895-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000514759.2:n.895-190_895-189insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000710265.1:c.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000518161.1:n.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000472832.3:c.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000483066.2:n.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000688158.2:n.1537-190_1537-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000688922.2:c.*632-190_*632-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000508742.2:n.*632-190_*632-189insGGCCGGGCGCGGTGGCTCACG...
ENST00000700021.1:c.757-190_757-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000514757.1:n.757-190_757-189insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000700022.1:c.*141-190_*141-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000514758.1:n.*141-190_*141-189insGGCCGGGCGCGGTGGCTCACG...
ENST00000700023.1:n.1960-190_1960-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000700024.1:n.2194-190_2194-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000700025.1:n.1571-190_1571-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000700026.1:n.439-190_439-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000700029.1:c.729-190_729-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000706954.1:c.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000516674.1:n.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000706955.1:c.*837-190_*837-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000516675.1:n.*837-190_*837-189insGGCCGGGCGCGGTGGCTCACG...
ENST00000686459.1:c.*388-190_*388-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000508909.1:n.*388-190_*388-189insGGCCGGGCGCGGTGGCTCACG...
ENST00000688158.1:c.*913-190_*913-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000509254.1:n.*913-190_*913-189insGGCCGGGCGCGGTGGCTCACG...
ENST00000688308.1:c.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000508752.1:n.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000688922.1:c.723-190_723-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000693560.1:c.1321-190_1321-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000509861.1:n.1321-190_1321-189insGGCCGGGCGCGGTGGCTCACG...
ENST00000371953.8:c.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG MANE Select ENSP00000361021.3:n.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000371953.7:c.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000361021.3:n.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000472832.2:c.229-190_229-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ENSP00000483066.1:n.229-190_229-189insGGCCGGGCGCGGTGGCTCACGCC...
NM_000314.5:c.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG NP_000305.3:n.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAAT...
NM_000314.6:c.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG NP_000305.3:n.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAAT...
NM_001304717.2:c.1321-190_1321-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG NP_001291646.2:n.1321-190_1321-189insGGCCGGGCGCGGTGGCTCACGCCT...
NM_001304718.1:c.211-190_211-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG NP_001291647.1:n.211-190_211-189insGGCCGGGCGCGGTGGCTCACGCCTGT...
XM_006717926.2:c.757-190_757-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG XP_006717989.1:n.757-190_757-189insGGCCGGGCGCGGTGGCTCACGCCTGT...
XM_011539981.1:c.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG XP_011538283.1:n.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGT...
XM_011539982.1:c.706-190_706-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG XP_011538284.1:n.706-190_706-189insGGCCGGGCGCGGTGGCTCACGCCTGT...
XR_945791.1:n.1372-190_1372-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
NM_000314.7:c.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG NP_000305.3:n.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAAT...
NM_001304717.5:c.1321-190_1321-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG NP_001291646.4:n.1321-190_1321-189insGGCCGGGCGCGGTGGCTCACGCCT...
NM_001304718.2:c.211-190_211-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG NP_001291647.1:n.211-190_211-189insGGCCGGGCGCGGTGGCTCACGCCTGT...
NM_000314.8:c.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG MANE Select NP_000305.3:n.802-190_802-189insGGCCGGGCGCGGTGGCTCACGCCTGTAAT...