Canonical Allele Identifier: CA1926189916
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960876_87960884delinsCTTTTTTTT , CM000672.2:g.87960876_87960884delinsCTTTTTTTT GRCh38
NC_000010.10:g.89720633_89720641delinsCTTTTTTTT , CM000672.1:g.89720633_89720641delinsCTTTTTTTT GRCh37
NC_000010.9:g.89710613_89710621delinsCTTTTTTTT NCBI36
NG_007466.2:g.102438_102446delinsCTTTTTTTT , LRG_311:g.102438_102446delinsCTTTTTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.895-18_895-10delinsCTTTTTTTT ENSP00000514759.2:n.895-18_895-10delinsCT...
ENST00000710265.1:c.802-18_802-10delinsCTTTTTTTT ENSP00000518161.1:n.802-18_802-10delinsCT...
ENST00000472832.3:c.802-18_802-10delinsCTTTTTTTT ENSP00000483066.2:n.802-18_802-10delinsCT...
ENST00000688158.2:n.1537-18_1537-10delinsCTTTTTTTT
ENST00000688922.2:c.*632-18_*632-10delinsCTTTTTTTT ENSP00000508742.2:n.*632-18_*632-10delins...
ENST00000700021.1:c.757-18_757-10delinsCTTTTTTTT ENSP00000514757.1:n.757-18_757-10delinsCT...
ENST00000700022.1:c.*141-18_*141-10delinsCTTTTTTTT ENSP00000514758.1:n.*141-18_*141-10delins...
ENST00000700023.1:n.1960-18_1960-10delinsCTTTTTTTT
ENST00000700024.1:n.2194-18_2194-10delinsCTTTTTTTT
ENST00000700025.1:n.1571-18_1571-10delinsCTTTTTTTT
ENST00000700026.1:n.439-18_439-10delinsCTTTTTTTT
ENST00000700029.1:c.729-18_729-10delinsCTTTTTTTT
ENST00000706954.1:c.802-18_802-10delinsCTTTTTTTT ENSP00000516674.1:n.802-18_802-10delinsCT...
ENST00000706955.1:c.*837-18_*837-10delinsCTTTTTTTT ENSP00000516675.1:n.*837-18_*837-10delins...
ENST00000686459.1:c.*388-18_*388-10delinsCTTTTTTTT ENSP00000508909.1:n.*388-18_*388-10delins...
ENST00000688158.1:c.*913-18_*913-10delinsCTTTTTTTT ENSP00000509254.1:n.*913-18_*913-10delins...
ENST00000688308.1:c.802-18_802-10delinsCTTTTTTTT ENSP00000508752.1:n.802-18_802-10delinsCT...
ENST00000688922.1:c.723-18_723-10delinsCTTTTTTTT
ENST00000693560.1:c.1321-18_1321-10delinsCTTTTTTTT ENSP00000509861.1:n.1321-18_1321-10delins...
ENST00000371953.8:c.802-18_802-10delinsCTTTTTTTT MANE Select ENSP00000361021.3:n.802-18_802-10delinsCT...
ENST00000371953.7:c.802-18_802-10delinsCTTTTTTTT ENSP00000361021.3:n.802-18_802-10delinsCT...
ENST00000472832.2:c.229-18_229-10delinsCTTTTTTTT ENSP00000483066.1:n.229-18_229-10delinsCT...
NM_000314.5:c.802-18_802-10delinsCTTTTTTTT NP_000305.3:n.802-18_802-10delinsCTTTTTTT...
NM_000314.6:c.802-18_802-10delinsCTTTTTTTT NP_000305.3:n.802-18_802-10delinsCTTTTTTT...
NM_001304717.2:c.1321-18_1321-10delinsCTTTTTTTT NP_001291646.2:n.1321-18_1321-10delinsCTT...
NM_001304718.1:c.211-18_211-10delinsCTTTTTTTT NP_001291647.1:n.211-18_211-10delinsCTTTT...
XM_006717926.2:c.757-18_757-10delinsCTTTTTTTT XP_006717989.1:n.757-18_757-10delinsCTTTT...
XM_011539981.1:c.802-18_802-10delinsCTTTTTTTT XP_011538283.1:n.802-18_802-10delinsCTTTT...
XM_011539982.1:c.706-18_706-10delinsCTTTTTTTT XP_011538284.1:n.706-18_706-10delinsCTTTT...
XR_945791.1:n.1372-18_1372-10delinsCTTTTTTTT
NM_000314.7:c.802-18_802-10delinsCTTTTTTTT NP_000305.3:n.802-18_802-10delinsCTTTTTTT...
NM_001304717.5:c.1321-18_1321-10delinsCTTTTTTTT NP_001291646.4:n.1321-18_1321-10delinsCTT...
NM_001304718.2:c.211-18_211-10delinsCTTTTTTTT NP_001291647.1:n.211-18_211-10delinsCTTTT...
NM_000314.8:c.802-18_802-10delinsCTTTTTTTT MANE Select NP_000305.3:n.802-18_802-10delinsCTTTTTTT...