Canonical Allele Identifier: CA2580610837
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108302899del , CM000673.2:g.108302899del GRCh38
NC_000011.9:g.108173626del , CM000673.1:g.108173626del GRCh37
NC_000011.8:g.107678836del NCBI36
NG_009830.1:g.85068del , LRG_135:g.85068del

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.5366del ENSP00000388058.2:p.Leu1789ArgfsTer4
ENST00000713593.1:c.*4837del ENSP00000518889.1:n.*4837del
ENST00000278616.9:c.5366del ENSP00000278616.4:p.Leu1789ArgfsTer4
ENST00000683174.1:n.6850del
ENST00000683524.1:n.590del
ENST00000684152.1:n.1080del
ENST00000527805.6:c.*430del ENSP00000435747.2:n.*430del
ENST00000675595.1:c.*430del ENSP00000502563.1:n.*430del
ENST00000675843.1:c.5366del MANE Select ENSP00000501606.1:p.Leu1789ArgfsTer4
ENST00000278616.8:c.5366del ENSP00000278616.4:p.Leu1789ArgfsTer4
ENST00000452508.6:c.5366del ENSP00000388058.2:p.Leu1789ArgfsTer4
ENST00000524792.5:n.1581del
ENST00000533690.5:n.770del
ENST00000534625.1:n.595del
NM_000051.3:c.5366del , LRG_135t1:c.5366del NP_000042.3:p.Leu1789ArgfsTer4
XM_005271561.3:c.5366del XP_005271618.2:p.Leu1789ArgfsTer4
XM_005271562.3:c.5366del XP_005271619.2:p.Leu1789ArgfsTer4
XM_006718843.2:c.5366del XP_006718906.1:p.Leu1789ArgfsTer4
XM_006718845.1:c.1322del XP_006718908.1:p.Leu441ArgfsTer4
XM_011542840.1:c.5366del XP_011541142.1:p.Leu1789ArgfsTer4
XM_011542841.1:c.5366del XP_011541143.1:p.Leu1789ArgfsTer4
XM_011542842.1:c.5201del XP_011541144.1:p.Leu1734ArgfsTer4
XM_011542843.1:c.5366del XP_011541145.1:p.Leu1789ArgfsTer4
XM_011542844.1:c.4322del XP_011541146.1:p.Leu1441ArgfsTer4
XM_011542845.1:c.4058del XP_011541147.1:p.Leu1353ArgfsTer4
XM_011542846.1:c.*24del XP_011541148.1:n.*24del
XM_011542847.1:c.437del XP_011541149.1:p.Leu146ArgfsTer4
NM_001351834.1:c.5366del NP_001338763.1:p.Leu1789ArgfsTer4
XM_005271562.5:c.5366del XP_005271619.2:p.Leu1789ArgfsTer4
XM_006718843.4:c.5366del XP_006718906.1:p.Leu1789ArgfsTer4
XM_006718845.2:c.1322del XP_006718908.1:p.Leu441ArgfsTer4
XM_011542840.3:c.5366del XP_011541142.1:p.Leu1789ArgfsTer4
XM_011542842.3:c.5201del XP_011541144.1:p.Leu1734ArgfsTer4
XM_011542843.2:c.5366del XP_011541145.1:p.Leu1789ArgfsTer4
XM_011542844.3:c.4322del XP_011541146.1:p.Leu1441ArgfsTer4
XM_011542845.2:c.4058del XP_011541147.1:p.Leu1353ArgfsTer4
XM_017017789.2:c.5366del XP_016873278.1:p.Leu1789ArgfsTer4
XM_017017790.2:c.5366del XP_016873279.1:p.Leu1789ArgfsTer4
XM_017017791.1:c.5366del XP_016873280.1:p.Leu1789ArgfsTer4
XM_017017792.2:c.*47del XP_016873281.1:n.*47del
XR_002957150.1:n.5966del
NM_001351834.2:c.5366del NP_001338763.1:p.Leu1789ArgfsTer4
NM_000051.4:c.5366del MANE Select NP_000042.3:p.Leu1789ArgfsTer4