Canonical Allele Identifier: CA891841316
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87952160_87952161delinsTT , CM000672.2:g.87952160_87952161delinsTT GRCh38
NC_000010.10:g.89711917_89711918delinsTT , CM000672.1:g.89711917_89711918delinsTT GRCh37
NC_000010.9:g.89701897_89701898delinsTT NCBI36
NG_007466.2:g.93722_93723delinsTT , LRG_311:g.93722_93723delinsTT

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.535_536delinsTT ENSP00000514759.2:p.Ser179Phe
ENST00000710265.1:c.535_536delinsTT ENSP00000518161.1:p.Ser179Phe
ENST00000472832.3:c.535_536delinsTT ENSP00000483066.2:p.Ser179Phe
ENST00000688158.2:n.1270_1271delinsTT
ENST00000688922.2:c.*365_*366delinsTT ENSP00000508742.2:n.*365_*366delinsTT
ENST00000700021.1:c.490_491delinsTT ENSP00000514757.1:p.Ser164Phe
ENST00000700022.1:c.493-5693_493-5692delinsTT ENSP00000514758.1:n.493-5693_493-5692deli...
ENST00000700023.1:n.1693_1694delinsTT
ENST00000700024.1:n.1927_1928delinsTT
ENST00000700025.1:n.1304_1305delinsTT
ENST00000700029.1:c.369_370delinsTT
ENST00000706954.1:c.535_536delinsTT ENSP00000516674.1:p.Ser179Phe
ENST00000706955.1:c.*570_*571delinsTT ENSP00000516675.1:n.*570_*571delinsTT
ENST00000686459.1:c.*121_*122delinsTT ENSP00000508909.1:n.*121_*122delinsTT
ENST00000688158.1:c.*646_*647delinsTT ENSP00000509254.1:n.*646_*647delinsTT
ENST00000688308.1:c.535_536delinsTT ENSP00000508752.1:p.Ser179Phe
ENST00000688922.1:c.456_457delinsTT
ENST00000693560.1:c.1054_1055delinsTT ENSP00000509861.1:p.Ser352Phe
ENST00000371953.8:c.535_536delinsTT MANE Select ENSP00000361021.3:p.Ser179Phe
ENST00000371953.7:c.535_536delinsTT ENSP00000361021.3:p.Ser179Phe
NM_000314.5:c.535_536delinsTT NP_000305.3:p.Ser179Phe
NM_000314.6:c.535_536delinsTT NP_000305.3:p.Ser179Phe
NM_001304717.2:c.1054_1055delinsTT NP_001291646.2:p.Ser352Phe
NM_001304718.1:c.-57_-56delinsTT NP_001291647.1:n.-57_-56delinsTT
XM_006717926.2:c.490_491delinsTT XP_006717989.1:p.Ser164Phe
XM_011539981.1:c.535_536delinsTT XP_011538283.1:p.Ser179Phe
XM_011539982.1:c.439_440delinsTT XP_011538284.1:p.Ser147Phe
XR_945789.1:n.1406_1407delinsTT
XR_945790.1:n.1523_1524delinsTT
XR_945791.1:n.1205-5693_1205-5692delinsTT
NM_000314.7:c.535_536delinsTT NP_000305.3:p.Ser179Phe
NM_001304717.5:c.1054_1055delinsTT NP_001291646.4:p.Ser352Phe
NM_001304718.2:c.-57_-56delinsTT NP_001291647.1:n.-57_-56delinsTT
NM_000314.8:c.535_536delinsTT MANE Select NP_000305.3:p.Ser179Phe