Canonical Allele Identifier: CA891835779
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87864504_87864505delinsTT , CM000672.2:g.87864504_87864505delinsTT GRCh38
NC_000010.10:g.89624261_89624262delinsTT , CM000672.1:g.89624261_89624262delinsTT GRCh37
NC_000010.9:g.89614241_89614242delinsTT NCBI36
NG_007466.2:g.6066_6067delinsTT , LRG_311:g.6066_6067delinsTT
NG_033079.1:g.3933_3934delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.35_36delinsTT ENSP00000514759.2:p.Asn12Ile
ENST00000710265.1:c.35_36delinsTT ENSP00000518161.1:p.Asn12Ile
ENST00000472832.3:c.35_36delinsTT ENSP00000483066.2:p.Asn12Ile
ENST00000688922.2:c.35_36delinsTT ENSP00000508742.2:p.Asn12Ile
ENST00000700021.1:c.35_36delinsTT ENSP00000514757.1:p.Asn12Ile
ENST00000700022.1:c.35_36delinsTT ENSP00000514758.1:p.Asn12Ile
ENST00000706954.1:c.35_36delinsTT ENSP00000516674.1:p.Asn12Ile
ENST00000706955.1:c.35_36delinsTT ENSP00000516675.1:p.Asn12Ile
ENST00000686459.1:c.35_36delinsTT ENSP00000508909.1:p.Asn12Ile
ENST00000688158.1:c.35_36delinsTT ENSP00000509254.1:p.Asn12Ile
ENST00000688308.1:c.35_36delinsTT ENSP00000508752.1:p.Asn12Ile
ENST00000693560.1:c.554_555delinsTT ENSP00000509861.1:p.Asn185Ile
ENST00000371953.8:c.35_36delinsTT MANE Select ENSP00000361021.3:p.Asn12Ile
ENST00000371953.7:c.35_36delinsTT ENSP00000361021.3:p.Asn12Ile
ENST00000462694.1:n.37_38delinsTT
ENST00000487939.1:n.56_57delinsTT
ENST00000610634.1:c.-68_-67delinsTT ENSP00000477517.1:n.-68_-67delinsTT
ENST00000618586.1:n.4_5delinsTT
NM_000314.5:c.35_36delinsTT NP_000305.3:p.Asn12Ile
NM_000314.6:c.35_36delinsTT NP_000305.3:p.Asn12Ile
NM_001304717.2:c.554_555delinsTT NP_001291646.2:p.Asn185Ile
NM_001304718.1:c.-671_-670delinsTT NP_001291647.1:n.-671_-670delinsTT
XM_006717926.2:c.35_36delinsTT XP_006717989.1:p.Asn12Ile
XM_011539981.1:c.35_36delinsTT XP_011538283.1:p.Asn12Ile
XR_945789.1:n.747_748delinsTT
XR_945790.1:n.747_748delinsTT
XR_945791.1:n.747_748delinsTT
NM_000314.7:c.35_36delinsTT NP_000305.3:p.Asn12Ile
NM_001304717.5:c.554_555delinsTT NP_001291646.4:p.Asn185Ile
NM_001304718.2:c.-671_-670delinsTT NP_001291647.1:n.-671_-670delinsTT
NM_000314.8:c.35_36delinsTT MANE Select NP_000305.3:p.Asn12Ile