Canonical Allele Identifier: CA891835773
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87864504_87864505delinsCT , CM000672.2:g.87864504_87864505delinsCT GRCh38
NC_000010.10:g.89624261_89624262delinsCT , CM000672.1:g.89624261_89624262delinsCT GRCh37
NC_000010.9:g.89614241_89614242delinsCT NCBI36
NG_007466.2:g.6066_6067delinsCT , LRG_311:g.6066_6067delinsCT
NG_033079.1:g.3933_3934delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.35_36delinsCT ENSP00000514759.2:p.Asn12Thr
ENST00000710265.1:c.35_36delinsCT ENSP00000518161.1:p.Asn12Thr
ENST00000472832.3:c.35_36delinsCT ENSP00000483066.2:p.Asn12Thr
ENST00000688922.2:c.35_36delinsCT ENSP00000508742.2:p.Asn12Thr
ENST00000700021.1:c.35_36delinsCT ENSP00000514757.1:p.Asn12Thr
ENST00000700022.1:c.35_36delinsCT ENSP00000514758.1:p.Asn12Thr
ENST00000706954.1:c.35_36delinsCT ENSP00000516674.1:p.Asn12Thr
ENST00000706955.1:c.35_36delinsCT ENSP00000516675.1:p.Asn12Thr
ENST00000686459.1:c.35_36delinsCT ENSP00000508909.1:p.Asn12Thr
ENST00000688158.1:c.35_36delinsCT ENSP00000509254.1:p.Asn12Thr
ENST00000688308.1:c.35_36delinsCT ENSP00000508752.1:p.Asn12Thr
ENST00000693560.1:c.554_555delinsCT ENSP00000509861.1:p.Asn185Thr
ENST00000371953.8:c.35_36delinsCT MANE Select ENSP00000361021.3:p.Asn12Thr
ENST00000371953.7:c.35_36delinsCT ENSP00000361021.3:p.Asn12Thr
ENST00000462694.1:n.37_38delinsCT
ENST00000487939.1:n.56_57delinsCT
ENST00000610634.1:c.-68_-67delinsCT ENSP00000477517.1:n.-68_-67delinsCT
ENST00000618586.1:n.4_5delinsCT
NM_000314.5:c.35_36delinsCT NP_000305.3:p.Asn12Thr
NM_000314.6:c.35_36delinsCT NP_000305.3:p.Asn12Thr
NM_001304717.2:c.554_555delinsCT NP_001291646.2:p.Asn185Thr
NM_001304718.1:c.-671_-670delinsCT NP_001291647.1:n.-671_-670delinsCT
XM_006717926.2:c.35_36delinsCT XP_006717989.1:p.Asn12Thr
XM_011539981.1:c.35_36delinsCT XP_011538283.1:p.Asn12Thr
XR_945789.1:n.747_748delinsCT
XR_945790.1:n.747_748delinsCT
XR_945791.1:n.747_748delinsCT
NM_000314.7:c.35_36delinsCT NP_000305.3:p.Asn12Thr
NM_001304717.5:c.554_555delinsCT NP_001291646.4:p.Asn185Thr
NM_001304718.2:c.-671_-670delinsCT NP_001291647.1:n.-671_-670delinsCT
NM_000314.8:c.35_36delinsCT MANE Select NP_000305.3:p.Asn12Thr