Canonical Allele Identifier: CA2579926818
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957991_87957992delinsGT , CM000672.2:g.87957991_87957992delinsGT GRCh38
NC_000010.10:g.89717748_89717749delinsGT , CM000672.1:g.89717748_89717749delinsGT GRCh37
NC_000010.9:g.89707728_89707729delinsGT NCBI36
NG_007466.2:g.99553_99554delinsGT , LRG_311:g.99553_99554delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.773_774delinsGT ENSP00000514759.2:p.Phe258Cys
ENST00000710265.1:c.773_774delinsGT ENSP00000518161.1:p.Phe258Cys
ENST00000472832.3:c.773_774delinsGT ENSP00000483066.2:p.Phe258Cys
ENST00000688158.2:n.1508_1509delinsGT
ENST00000688922.2:c.*603_*604delinsGT ENSP00000508742.2:n.*603_*604delinsGT
ENST00000700021.1:c.728_729delinsGT ENSP00000514757.1:p.Phe243Cys
ENST00000700022.1:c.*112_*113delinsGT ENSP00000514758.1:n.*112_*113delinsGT
ENST00000700023.1:n.1931_1932delinsGT
ENST00000700024.1:n.2165_2166delinsGT
ENST00000700025.1:n.1542_1543delinsGT
ENST00000700026.1:n.410_411delinsGT
ENST00000700029.1:c.607_608delinsGT
ENST00000706954.1:c.773_774delinsGT ENSP00000516674.1:p.Phe258Cys
ENST00000706955.1:c.*808_*809delinsGT ENSP00000516675.1:n.*808_*809delinsGT
ENST00000686459.1:c.*359_*360delinsGT ENSP00000508909.1:n.*359_*360delinsGT
ENST00000688158.1:c.*884_*885delinsGT ENSP00000509254.1:n.*884_*885delinsGT
ENST00000688308.1:c.773_774delinsGT ENSP00000508752.1:p.Phe258Cys
ENST00000688922.1:c.694_695delinsGT
ENST00000693560.1:c.1292_1293delinsGT ENSP00000509861.1:p.Phe431Cys
ENST00000371953.8:c.773_774delinsGT MANE Select ENSP00000361021.3:p.Phe258Cys
ENST00000371953.7:c.773_774delinsGT ENSP00000361021.3:p.Phe258Cys
ENST00000472832.2:c.200_201delinsGT ENSP00000483066.1:p.Phe67Cys
NM_000314.5:c.773_774delinsGT NP_000305.3:p.Phe258Cys
NM_000314.6:c.773_774delinsGT NP_000305.3:p.Phe258Cys
NM_001304717.2:c.1292_1293delinsGT NP_001291646.2:p.Phe431Cys
NM_001304718.1:c.182_183delinsGT NP_001291647.1:p.Phe61Cys
XM_006717926.2:c.728_729delinsGT XP_006717989.1:p.Phe243Cys
XM_011539981.1:c.773_774delinsGT XP_011538283.1:p.Phe258Cys
XM_011539982.1:c.677_678delinsGT XP_011538284.1:p.Phe226Cys
XR_945791.1:n.1343_1344delinsGT
NM_000314.7:c.773_774delinsGT NP_000305.3:p.Phe258Cys
NM_001304717.5:c.1292_1293delinsGT NP_001291646.4:p.Phe431Cys
NM_001304718.2:c.182_183delinsGT NP_001291647.1:p.Phe61Cys
NM_000314.8:c.773_774delinsGT MANE Select NP_000305.3:p.Phe258Cys