Canonical Allele Identifier: CA2574970897
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108279494del , CM000673.2:g.108279494del GRCh38
NC_000011.9:g.108150221del , CM000673.1:g.108150221del GRCh37
NC_000011.8:g.107655431del NCBI36
NG_009830.1:g.61663del , LRG_135:g.61663del

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.3288del ENSP00000388058.2:p.Leu1096PhefsTer13
ENST00000713593.1:c.*2759del ENSP00000518889.1:n.*2759del
ENST00000278616.9:c.3288del ENSP00000278616.4:p.Leu1096PhefsTer13
ENST00000683174.1:n.3438del
ENST00000527805.6:c.3288del ENSP00000435747.2:p.Leu1096PhefsTer13
ENST00000675595.1:c.3123del ENSP00000502563.1:p.Leu1041PhefsTer13
ENST00000675843.1:c.3288del MANE Select ENSP00000501606.1:p.Leu1096PhefsTer13
ENST00000278616.8:c.3288del ENSP00000278616.4:p.Leu1096PhefsTer13
ENST00000452508.6:c.3288del ENSP00000388058.2:p.Leu1096PhefsTer13
ENST00000527805.5:c.3288del ENSP00000435747.1:p.Leu1096PhefsTer13
NM_000051.3:c.3288del , LRG_135t1:c.3288del NP_000042.3:p.Leu1096PhefsTer13
XM_005271561.3:c.3288del XP_005271618.2:p.Leu1096PhefsTer13
XM_005271562.3:c.3288del XP_005271619.2:p.Leu1096PhefsTer13
XM_006718843.2:c.3288del XP_006718906.1:p.Leu1096PhefsTer13
XM_011542840.1:c.3288del XP_011541142.1:p.Leu1096PhefsTer13
XM_011542841.1:c.3288del XP_011541143.1:p.Leu1096PhefsTer13
XM_011542842.1:c.3123del XP_011541144.1:p.Leu1041PhefsTer13
XM_011542843.1:c.3288del XP_011541145.1:p.Leu1096PhefsTer13
XM_011542844.1:c.2244del XP_011541146.1:p.Leu748PhefsTer13
XM_011542845.1:c.1980del XP_011541147.1:p.Leu660PhefsTer13
XM_011542846.1:c.3288del XP_011541148.1:p.Leu1096PhefsTer13
NM_001351834.1:c.3288del NP_001338763.1:p.Leu1096PhefsTer13
XM_005271562.5:c.3288del XP_005271619.2:p.Leu1096PhefsTer13
XM_006718843.4:c.3288del XP_006718906.1:p.Leu1096PhefsTer13
XM_011542840.3:c.3288del XP_011541142.1:p.Leu1096PhefsTer13
XM_011542842.3:c.3123del XP_011541144.1:p.Leu1041PhefsTer13
XM_011542843.2:c.3288del XP_011541145.1:p.Leu1096PhefsTer13
XM_011542844.3:c.2244del XP_011541146.1:p.Leu748PhefsTer13
XM_011542845.2:c.1980del XP_011541147.1:p.Leu660PhefsTer13
XM_017017789.2:c.3288del XP_016873278.1:p.Leu1096PhefsTer13
XM_017017790.2:c.3288del XP_016873279.1:p.Leu1096PhefsTer13
XM_017017791.1:c.3288del XP_016873280.1:p.Leu1096PhefsTer13
XM_017017792.2:c.3288del XP_016873281.1:p.Leu1096PhefsTer13
XR_002957150.1:n.4021del
NM_001351834.2:c.3288del NP_001338763.1:p.Leu1096PhefsTer13
NM_000051.4:c.3288del MANE Select NP_000042.3:p.Leu1096PhefsTer13