Canonical Allele Identifier: CA1926188606
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957989_87957991delinsCTT , CM000672.2:g.87957989_87957991delinsCTT GRCh38
NC_000010.10:g.89717746_89717748delinsCTT , CM000672.1:g.89717746_89717748delinsCTT GRCh37
NC_000010.9:g.89707726_89707728delinsCTT NCBI36
NG_007466.2:g.99551_99553delinsCTT , LRG_311:g.99551_99553delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.771_773delinsCTT ENSP00000514759.2:p.Phe257=
ENST00000710265.1:c.771_773delinsCTT ENSP00000518161.1:p.Phe257=
ENST00000472832.3:c.771_773delinsCTT ENSP00000483066.2:p.Phe257=
ENST00000688158.2:n.1506_1508delinsCTT
ENST00000688922.2:c.*601_*603delinsCTT ENSP00000508742.2:n.*601_*603delinsCTT
ENST00000700021.1:c.726_728delinsCTT ENSP00000514757.1:p.Phe242=
ENST00000700022.1:c.*110_*112delinsCTT ENSP00000514758.1:n.*110_*112delinsCTT
ENST00000700023.1:n.1929_1931delinsCTT
ENST00000700024.1:n.2163_2165delinsCTT
ENST00000700025.1:n.1540_1542delinsCTT
ENST00000700026.1:n.408_410delinsCTT
ENST00000700029.1:c.605_607delinsCTT
ENST00000706954.1:c.771_773delinsCTT ENSP00000516674.1:p.Phe257=
ENST00000706955.1:c.*806_*808delinsCTT ENSP00000516675.1:n.*806_*808delinsCTT
ENST00000686459.1:c.*357_*359delinsCTT ENSP00000508909.1:n.*357_*359delinsCTT
ENST00000688158.1:c.*882_*884delinsCTT ENSP00000509254.1:n.*882_*884delinsCTT
ENST00000688308.1:c.771_773delinsCTT ENSP00000508752.1:p.Phe257=
ENST00000688922.1:c.692_694delinsCTT
ENST00000693560.1:c.1290_1292delinsCTT ENSP00000509861.1:p.Phe430=
ENST00000371953.8:c.771_773delinsCTT MANE Select ENSP00000361021.3:p.Phe257=
ENST00000371953.7:c.771_773delinsCTT ENSP00000361021.3:p.Phe257=
ENST00000472832.2:c.198_200delinsCTT ENSP00000483066.1:p.Phe66=
NM_000314.5:c.771_773delinsCTT NP_000305.3:p.Phe257=
NM_000314.6:c.771_773delinsCTT NP_000305.3:p.Phe257=
NM_001304717.2:c.1290_1292delinsCTT NP_001291646.2:p.Phe430=
NM_001304718.1:c.180_182delinsCTT NP_001291647.1:p.Phe60=
XM_006717926.2:c.726_728delinsCTT XP_006717989.1:p.Phe242=
XM_011539981.1:c.771_773delinsCTT XP_011538283.1:p.Phe257=
XM_011539982.1:c.675_677delinsCTT XP_011538284.1:p.Phe225=
XR_945791.1:n.1341_1343delinsCTT
NM_000314.7:c.771_773delinsCTT NP_000305.3:p.Phe257=
NM_001304717.5:c.1290_1292delinsCTT NP_001291646.4:p.Phe430=
NM_001304718.2:c.180_182delinsCTT NP_001291647.1:p.Phe60=
NM_000314.8:c.771_773delinsCTT MANE Select NP_000305.3:p.Phe257=