Canonical Allele Identifier: CA1998799503
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108302816_108302818delinsTTC , CM000673.2:g.108302816_108302818delinsTTC GRCh38
NC_000011.9:g.108173543_108173545delinsTTC , CM000673.1:g.108173543_108173545delinsTTC GRCh37
NC_000011.8:g.107678753_107678755delinsTTC NCBI36
NG_009830.1:g.84985_84987delinsTTC , LRG_135:g.84985_84987delinsTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.5320-37_5320-35delinsTTC ENSP00000388058.2:n.5320-37_5320-35delins...
ENST00000713593.1:c.*4791-37_*4791-35delinsTTC ENSP00000518889.1:n.*4791-37_*4791-35deli...
ENST00000278616.9:c.5320-37_5320-35delinsTTC ENSP00000278616.4:n.5320-37_5320-35delins...
ENST00000683174.1:n.6804-37_6804-35delinsTTC
ENST00000683524.1:n.544-37_544-35delinsTTC
ENST00000684152.1:n.1034-37_1034-35delinsTTC
ENST00000527805.6:c.*384-37_*384-35delinsTTC ENSP00000435747.2:n.*384-37_*384-35delins...
ENST00000675595.1:c.*384-37_*384-35delinsTTC ENSP00000502563.1:n.*384-37_*384-35delins...
ENST00000675843.1:c.5320-37_5320-35delinsTTC MANE Select ENSP00000501606.1:n.5320-37_5320-35delins...
ENST00000278616.8:c.5320-37_5320-35delinsTTC ENSP00000278616.4:n.5320-37_5320-35delins...
ENST00000452508.6:c.5320-37_5320-35delinsTTC ENSP00000388058.2:n.5320-37_5320-35delins...
ENST00000524792.5:n.1535-37_1535-35delinsTTC
ENST00000533690.5:n.724-37_724-35delinsTTC
ENST00000534625.1:n.549-37_549-35delinsTTC
NM_000051.3:c.5320-37_5320-35delinsTTC , LRG_135t1:c.5320-37_5320-35delinsTTC NP_000042.3:n.5320-37_5320-35delinsTTC
XM_005271561.3:c.5320-37_5320-35delinsTTC XP_005271618.2:n.5320-37_5320-35delinsTTC...
XM_005271562.3:c.5320-37_5320-35delinsTTC XP_005271619.2:n.5320-37_5320-35delinsTTC...
XM_006718843.2:c.5320-37_5320-35delinsTTC XP_006718906.1:n.5320-37_5320-35delinsTTC...
XM_006718845.1:c.1276-37_1276-35delinsTTC XP_006718908.1:n.1276-37_1276-35delinsTTC...
XM_011542840.1:c.5320-37_5320-35delinsTTC XP_011541142.1:n.5320-37_5320-35delinsTTC...
XM_011542841.1:c.5320-37_5320-35delinsTTC XP_011541143.1:n.5320-37_5320-35delinsTTC...
XM_011542842.1:c.5155-37_5155-35delinsTTC XP_011541144.1:n.5155-37_5155-35delinsTTC...
XM_011542843.1:c.5320-37_5320-35delinsTTC XP_011541145.1:n.5320-37_5320-35delinsTTC...
XM_011542844.1:c.4276-37_4276-35delinsTTC XP_011541146.1:n.4276-37_4276-35delinsTTC...
XM_011542845.1:c.4012-37_4012-35delinsTTC XP_011541147.1:n.4012-37_4012-35delinsTTC...
XM_011542846.1:c.5319-35_5319-33delinsTTC XP_011541148.1:n.5319-35_5319-33delinsTTC...
XM_011542847.1:c.391-37_391-35delinsTTC XP_011541149.1:n.391-37_391-35delinsTTC
NM_001351834.1:c.5320-37_5320-35delinsTTC NP_001338763.1:n.5320-37_5320-35delinsTTC...
XM_005271562.5:c.5320-37_5320-35delinsTTC XP_005271619.2:n.5320-37_5320-35delinsTTC...
XM_006718843.4:c.5320-37_5320-35delinsTTC XP_006718906.1:n.5320-37_5320-35delinsTTC...
XM_006718845.2:c.1276-37_1276-35delinsTTC XP_006718908.1:n.1276-37_1276-35delinsTTC...
XM_011542840.3:c.5320-37_5320-35delinsTTC XP_011541142.1:n.5320-37_5320-35delinsTTC...
XM_011542842.3:c.5155-37_5155-35delinsTTC XP_011541144.1:n.5155-37_5155-35delinsTTC...
XM_011542843.2:c.5320-37_5320-35delinsTTC XP_011541145.1:n.5320-37_5320-35delinsTTC...
XM_011542844.3:c.4276-37_4276-35delinsTTC XP_011541146.1:n.4276-37_4276-35delinsTTC...
XM_011542845.2:c.4012-37_4012-35delinsTTC XP_011541147.1:n.4012-37_4012-35delinsTTC...
XM_017017789.2:c.5320-37_5320-35delinsTTC XP_016873278.1:n.5320-37_5320-35delinsTTC...
XM_017017790.2:c.5320-37_5320-35delinsTTC XP_016873279.1:n.5320-37_5320-35delinsTTC...
XM_017017791.1:c.5320-37_5320-35delinsTTC XP_016873280.1:n.5320-37_5320-35delinsTTC...
XM_017017792.2:c.*1-37_*1-35delinsTTC XP_016873281.1:n.*1-37_*1-35delinsTTC
XR_002957150.1:n.5920-37_5920-35delinsTTC
NM_001351834.2:c.5320-37_5320-35delinsTTC NP_001338763.1:n.5320-37_5320-35delinsTTC...
NM_000051.4:c.5320-37_5320-35delinsTTC MANE Select NP_000042.3:n.5320-37_5320-35delinsTTC