Canonical Allele Identifier: CA891840189
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960901_87960902delinsAA , CM000672.2:g.87960901_87960902delinsAA GRCh38
NC_000010.10:g.89720658_89720659delinsAA , CM000672.1:g.89720658_89720659delinsAA GRCh37
NC_000010.9:g.89710638_89710639delinsAA NCBI36
NG_007466.2:g.102463_102464delinsAA , LRG_311:g.102463_102464delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.902_903delinsAA ENSP00000514759.2:p.Met301Lys
ENST00000710265.1:c.809_810delinsAA ENSP00000518161.1:p.Met270Lys
ENST00000472832.3:c.809_810delinsAA ENSP00000483066.2:p.Met270Lys
ENST00000688158.2:n.1544_1545delinsAA
ENST00000688922.2:c.*639_*640delinsAA ENSP00000508742.2:n.*639_*640delinsAA
ENST00000700021.1:c.764_765delinsAA ENSP00000514757.1:p.Met255Lys
ENST00000700022.1:c.*148_*149delinsAA ENSP00000514758.1:n.*148_*149delinsAA
ENST00000700023.1:n.1967_1968delinsAA
ENST00000700024.1:n.2201_2202delinsAA
ENST00000700025.1:n.1578_1579delinsAA
ENST00000700026.1:n.446_447delinsAA
ENST00000700029.1:c.736_737delinsAA
ENST00000706954.1:c.809_810delinsAA ENSP00000516674.1:p.Met270Lys
ENST00000706955.1:c.*844_*845delinsAA ENSP00000516675.1:n.*844_*845delinsAA
ENST00000686459.1:c.*395_*396delinsAA ENSP00000508909.1:n.*395_*396delinsAA
ENST00000688158.1:c.*920_*921delinsAA ENSP00000509254.1:n.*920_*921delinsAA
ENST00000688308.1:c.809_810delinsAA ENSP00000508752.1:p.Met270Lys
ENST00000688922.1:c.730_731delinsAA
ENST00000693560.1:c.1328_1329delinsAA ENSP00000509861.1:p.Met443Lys
ENST00000371953.8:c.809_810delinsAA MANE Select ENSP00000361021.3:p.Met270Lys
ENST00000371953.7:c.809_810delinsAA ENSP00000361021.3:p.Met270Lys
ENST00000472832.2:c.236_237delinsAA ENSP00000483066.1:p.Met79Lys
NM_000314.5:c.809_810delinsAA NP_000305.3:p.Met270Lys
NM_000314.6:c.809_810delinsAA NP_000305.3:p.Met270Lys
NM_001304717.2:c.1328_1329delinsAA NP_001291646.2:p.Met443Lys
NM_001304718.1:c.218_219delinsAA NP_001291647.1:p.Met73Lys
XM_006717926.2:c.764_765delinsAA XP_006717989.1:p.Met255Lys
XM_011539981.1:c.809_810delinsAA XP_011538283.1:p.Met270Lys
XM_011539982.1:c.713_714delinsAA XP_011538284.1:p.Met238Lys
XR_945791.1:n.1379_1380delinsAA
NM_000314.7:c.809_810delinsAA NP_000305.3:p.Met270Lys
NM_001304717.5:c.1328_1329delinsAA NP_001291646.4:p.Met443Lys
NM_001304718.2:c.218_219delinsAA NP_001291647.1:p.Met73Lys
NM_000314.8:c.809_810delinsAA MANE Select NP_000305.3:p.Met270Lys