Canonical Allele Identifier: CA645569747
Gene: ATM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108257560_108257563del , CM000673.2:g.108257560_108257563del GRCh38
NC_000011.9:g.108128287_108128290del , CM000673.1:g.108128287_108128290del GRCh37
NC_000011.8:g.107633497_107633500del NCBI36
NG_009830.1:g.39729_39732del , LRG_135:g.39729_39732del

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.2330_2333del ENSP00000388058.2:p.Arg777IlefsTer2
ENST00000713593.1:c.*1801_*1804del ENSP00000518889.1:n.*1801_*1804del
ENST00000278616.9:c.2330_2333del ENSP00000278616.4:p.Arg777IlefsTer2
ENST00000682516.1:n.2464_2467del
ENST00000683174.1:n.2480_2483del
ENST00000683605.1:n.1825_1828del
ENST00000684037.1:c.*1265_*1268del ENSP00000508245.1:n.*1265_*1268del
ENST00000527805.6:c.2330_2333del ENSP00000435747.2:p.Arg777IlefsTer2
ENST00000675595.1:c.2165_2168del ENSP00000502563.1:p.Arg722IlefsTer2
ENST00000675843.1:c.2330_2333del MANE Select ENSP00000501606.1:p.Arg777IlefsTer2
ENST00000278616.8:c.2330_2333del ENSP00000278616.4:p.Arg777IlefsTer2
ENST00000452508.6:c.2330_2333del ENSP00000388058.2:p.Arg777IlefsTer2
ENST00000527805.5:c.2330_2333del ENSP00000435747.1:p.Arg777IlefsTer2
NM_000051.3:c.2330_2333del , LRG_135t1:c.2330_2333del NP_000042.3:p.Arg777IlefsTer2
XM_005271561.3:c.2330_2333del XP_005271618.2:p.Arg777IlefsTer2
XM_005271562.3:c.2330_2333del XP_005271619.2:p.Arg777IlefsTer2
XM_006718843.2:c.2330_2333del XP_006718906.1:p.Arg777IlefsTer2
XM_011542840.1:c.2330_2333del XP_011541142.1:p.Arg777IlefsTer2
XM_011542841.1:c.2330_2333del XP_011541143.1:p.Arg777IlefsTer2
XM_011542842.1:c.2165_2168del XP_011541144.1:p.Arg722IlefsTer2
XM_011542843.1:c.2330_2333del XP_011541145.1:p.Arg777IlefsTer2
XM_011542844.1:c.1286_1289del XP_011541146.1:p.Arg429IlefsTer2
XM_011542845.1:c.1022_1025del XP_011541147.1:p.Arg341IlefsTer2
XM_011542846.1:c.2330_2333del XP_011541148.1:p.Arg777IlefsTer2
NM_001351834.1:c.2330_2333del NP_001338763.1:p.Arg777IlefsTer2
XM_005271562.5:c.2330_2333del XP_005271619.2:p.Arg777IlefsTer2
XM_006718843.4:c.2330_2333del XP_006718906.1:p.Arg777IlefsTer2
XM_011542840.3:c.2330_2333del XP_011541142.1:p.Arg777IlefsTer2
XM_011542842.3:c.2165_2168del XP_011541144.1:p.Arg722IlefsTer2
XM_011542843.2:c.2330_2333del XP_011541145.1:p.Arg777IlefsTer2
XM_011542844.3:c.1286_1289del XP_011541146.1:p.Arg429IlefsTer2
XM_011542845.2:c.1022_1025del XP_011541147.1:p.Arg341IlefsTer2
XM_017017789.2:c.2330_2333del XP_016873278.1:p.Arg777IlefsTer2
XM_017017790.2:c.2330_2333del XP_016873279.1:p.Arg777IlefsTer2
XM_017017791.1:c.2330_2333del XP_016873280.1:p.Arg777IlefsTer2
XM_017017792.2:c.2330_2333del XP_016873281.1:p.Arg777IlefsTer2
XR_002957150.1:n.3063_3066del
NM_001351834.2:c.2330_2333del NP_001338763.1:p.Arg777IlefsTer2
NM_000051.4:c.2330_2333del MANE Select NP_000042.3:p.Arg777IlefsTer2