Canonical Allele Identifier: CA891835727
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960991_87960992delinsGA , CM000672.2:g.87960991_87960992delinsGA GRCh38
NC_000010.10:g.89720748_89720749delinsGA , CM000672.1:g.89720748_89720749delinsGA GRCh37
NC_000010.9:g.89710728_89710729delinsGA NCBI36
NG_007466.2:g.102553_102554delinsGA , LRG_311:g.102553_102554delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.992_993delinsGA ENSP00000514759.2:p.Ile331Arg
ENST00000710265.1:c.899_900delinsGA ENSP00000518161.1:p.Ile300Arg
ENST00000472832.3:c.899_900delinsGA ENSP00000483066.2:p.Ile300Arg
ENST00000688158.2:n.1634_1635delinsGA
ENST00000688922.2:c.*729_*730delinsGA ENSP00000508742.2:n.*729_*730delinsGA
ENST00000700021.1:c.854_855delinsGA ENSP00000514757.1:p.Ile285Arg
ENST00000700022.1:c.*238_*239delinsGA ENSP00000514758.1:n.*238_*239delinsGA
ENST00000700023.1:n.2057_2058delinsGA
ENST00000700024.1:n.2291_2292delinsGA
ENST00000700025.1:n.1668_1669delinsGA
ENST00000700026.1:n.536_537delinsGA
ENST00000706954.1:c.899_900delinsGA ENSP00000516674.1:p.Ile300Arg
ENST00000706955.1:c.*934_*935delinsGA ENSP00000516675.1:n.*934_*935delinsGA
ENST00000686459.1:c.*485_*486delinsGA ENSP00000508909.1:n.*485_*486delinsGA
ENST00000688158.1:c.*1010_*1011delinsGA ENSP00000509254.1:n.*1010_*1011delinsGA
ENST00000688308.1:c.899_900delinsGA ENSP00000508752.1:p.Ile300Arg
ENST00000688922.1:c.820_821delinsGA
ENST00000693560.1:c.1418_1419delinsGA ENSP00000509861.1:p.Ile473Arg
ENST00000371953.8:c.899_900delinsGA MANE Select ENSP00000361021.3:p.Ile300Arg
ENST00000371953.7:c.899_900delinsGA ENSP00000361021.3:p.Ile300Arg
ENST00000472832.2:c.326_327delinsGA ENSP00000483066.1:p.Ile109Arg
NM_000314.5:c.899_900delinsGA NP_000305.3:p.Ile300Arg
NM_000314.6:c.899_900delinsGA NP_000305.3:p.Ile300Arg
NM_001304717.2:c.1418_1419delinsGA NP_001291646.2:p.Ile473Arg
NM_001304718.1:c.308_309delinsGA NP_001291647.1:p.Ile103Arg
XM_006717926.2:c.854_855delinsGA XP_006717989.1:p.Ile285Arg
XM_011539981.1:c.899_900delinsGA XP_011538283.1:p.Ile300Arg
XM_011539982.1:c.803_804delinsGA XP_011538284.1:p.Ile268Arg
XR_945791.1:n.1469_1470delinsGA
NM_000314.7:c.899_900delinsGA NP_000305.3:p.Ile300Arg
NM_001304717.5:c.1418_1419delinsGA NP_001291646.4:p.Ile473Arg
NM_001304718.2:c.308_309delinsGA NP_001291647.1:p.Ile103Arg
NM_000314.8:c.899_900delinsGA MANE Select NP_000305.3:p.Ile300Arg