Canonical Allele Identifier: CA1926189871
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960839_87960878delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT , CM000672.2:g.87960839_87960878delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT GRCh38
NC_000010.10:g.89720596_89720635delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT , CM000672.1:g.89720596_89720635delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT GRCh37
NC_000010.9:g.89710576_89710615delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT NCBI36
NG_007466.2:g.102401_102440delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT , LRG_311:g.102401_102440delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.895-55_895-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000514759.2:n.895-55_895-16delinsCA...
ENST00000710265.1:c.802-55_802-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000518161.1:n.802-55_802-16delinsCA...
ENST00000472832.3:c.802-55_802-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000483066.2:n.802-55_802-16delinsCA...
ENST00000688158.2:n.1537-55_1537-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT
ENST00000688922.2:c.*632-55_*632-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000508742.2:n.*632-55_*632-16delins...
ENST00000700021.1:c.757-55_757-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000514757.1:n.757-55_757-16delinsCA...
ENST00000700022.1:c.*141-55_*141-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000514758.1:n.*141-55_*141-16delins...
ENST00000700023.1:n.1960-55_1960-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT
ENST00000700024.1:n.2194-55_2194-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT
ENST00000700025.1:n.1571-55_1571-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT
ENST00000700026.1:n.439-55_439-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT
ENST00000700029.1:c.729-55_729-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT
ENST00000706954.1:c.802-55_802-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000516674.1:n.802-55_802-16delinsCA...
ENST00000706955.1:c.*837-55_*837-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000516675.1:n.*837-55_*837-16delins...
ENST00000686459.1:c.*388-55_*388-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000508909.1:n.*388-55_*388-16delins...
ENST00000688158.1:c.*913-55_*913-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000509254.1:n.*913-55_*913-16delins...
ENST00000688308.1:c.802-55_802-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000508752.1:n.802-55_802-16delinsCA...
ENST00000688922.1:c.723-55_723-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT
ENST00000693560.1:c.1321-55_1321-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000509861.1:n.1321-55_1321-16delins...
ENST00000371953.8:c.802-55_802-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT MANE Select ENSP00000361021.3:n.802-55_802-16delinsCA...
ENST00000371953.7:c.802-55_802-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000361021.3:n.802-55_802-16delinsCA...
ENST00000472832.2:c.229-55_229-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT ENSP00000483066.1:n.229-55_229-16delinsCA...
NM_000314.5:c.802-55_802-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT NP_000305.3:n.802-55_802-16delinsCATTAATT...
NM_000314.6:c.802-55_802-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT NP_000305.3:n.802-55_802-16delinsCATTAATT...
NM_001304717.2:c.1321-55_1321-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT NP_001291646.2:n.1321-55_1321-16delinsCAT...
NM_001304718.1:c.211-55_211-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT NP_001291647.1:n.211-55_211-16delinsCATTA...
XM_006717926.2:c.757-55_757-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT XP_006717989.1:n.757-55_757-16delinsCATTA...
XM_011539981.1:c.802-55_802-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT XP_011538283.1:n.802-55_802-16delinsCATTA...
XM_011539982.1:c.706-55_706-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT XP_011538284.1:n.706-55_706-16delinsCATTA...
XR_945791.1:n.1372-55_1372-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT
NM_000314.7:c.802-55_802-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT NP_000305.3:n.802-55_802-16delinsCATTAATT...
NM_001304717.5:c.1321-55_1321-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT NP_001291646.4:n.1321-55_1321-16delinsCAT...
NM_001304718.2:c.211-55_211-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT NP_001291647.1:n.211-55_211-16delinsCATTA...
NM_000314.8:c.802-55_802-16delinsCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTT MANE Select NP_000305.3:n.802-55_802-16delinsCATTAATT...