Canonical Allele Identifier: CA891840898
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957990_87957991delinsGC , CM000672.2:g.87957990_87957991delinsGC GRCh38
NC_000010.10:g.89717747_89717748delinsGC , CM000672.1:g.89717747_89717748delinsGC GRCh37
NC_000010.9:g.89707727_89707728delinsGC NCBI36
NG_007466.2:g.99552_99553delinsGC , LRG_311:g.99552_99553delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.772_773delinsGC ENSP00000514759.2:p.Phe258Ala
ENST00000710265.1:c.772_773delinsGC ENSP00000518161.1:p.Phe258Ala
ENST00000472832.3:c.772_773delinsGC ENSP00000483066.2:p.Phe258Ala
ENST00000688158.2:n.1507_1508delinsGC
ENST00000688922.2:c.*602_*603delinsGC ENSP00000508742.2:n.*602_*603delinsGC
ENST00000700021.1:c.727_728delinsGC ENSP00000514757.1:p.Phe243Ala
ENST00000700022.1:c.*111_*112delinsGC ENSP00000514758.1:n.*111_*112delinsGC
ENST00000700023.1:n.1930_1931delinsGC
ENST00000700024.1:n.2164_2165delinsGC
ENST00000700025.1:n.1541_1542delinsGC
ENST00000700026.1:n.409_410delinsGC
ENST00000700029.1:c.606_607delinsGC
ENST00000706954.1:c.772_773delinsGC ENSP00000516674.1:p.Phe258Ala
ENST00000706955.1:c.*807_*808delinsGC ENSP00000516675.1:n.*807_*808delinsGC
ENST00000686459.1:c.*358_*359delinsGC ENSP00000508909.1:n.*358_*359delinsGC
ENST00000688158.1:c.*883_*884delinsGC ENSP00000509254.1:n.*883_*884delinsGC
ENST00000688308.1:c.772_773delinsGC ENSP00000508752.1:p.Phe258Ala
ENST00000688922.1:c.693_694delinsGC
ENST00000693560.1:c.1291_1292delinsGC ENSP00000509861.1:p.Phe431Ala
ENST00000371953.8:c.772_773delinsGC MANE Select ENSP00000361021.3:p.Phe258Ala
ENST00000371953.7:c.772_773delinsGC ENSP00000361021.3:p.Phe258Ala
ENST00000472832.2:c.199_200delinsGC ENSP00000483066.1:p.Phe67Ala
NM_000314.5:c.772_773delinsGC NP_000305.3:p.Phe258Ala
NM_000314.6:c.772_773delinsGC NP_000305.3:p.Phe258Ala
NM_001304717.2:c.1291_1292delinsGC NP_001291646.2:p.Phe431Ala
NM_001304718.1:c.181_182delinsGC NP_001291647.1:p.Phe61Ala
XM_006717926.2:c.727_728delinsGC XP_006717989.1:p.Phe243Ala
XM_011539981.1:c.772_773delinsGC XP_011538283.1:p.Phe258Ala
XM_011539982.1:c.676_677delinsGC XP_011538284.1:p.Phe226Ala
XR_945791.1:n.1342_1343delinsGC
NM_000314.7:c.772_773delinsGC NP_000305.3:p.Phe258Ala
NM_001304717.5:c.1291_1292delinsGC NP_001291646.4:p.Phe431Ala
NM_001304718.2:c.181_182delinsGC NP_001291647.1:p.Phe61Ala
NM_000314.8:c.772_773delinsGC MANE Select NP_000305.3:p.Phe258Ala