Canonical Allele Identifier: CA658821426
Community Standard Title: NM_000051.4(ATM):c.1259_1264del (p.Ile420_Ser421del)
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108250724_108250729del , CM000673.2:g.108250724_108250729del GRCh38
NC_000011.9:g.108121451_108121456del , CM000673.1:g.108121451_108121456del GRCh37
NC_000011.8:g.107626661_107626666del NCBI36
NG_009830.1:g.32893_32898del , LRG_135:g.32893_32898del

Transcript Alleles

HGVS Amino-acid Change
NM_000051.4:c.1259_1264del MANE Select NP_000042.3:p.Ile420_Ser421del
ENST00000675843.1:c.1259_1264del MANE Select ENSP00000501606.1:p.Ile420_Ser421del
NM_000051.3:c.1259_1264del , LRG_135t1:c.1259_1264del NP_000042.3:p.Ile420_Ser421del
NM_001351834.1:c.1259_1264del NP_001338763.1:p.Ile420_Ser421del
NM_001351834.2:c.1259_1264del NP_001338763.1:p.Ile420_Ser421del
ENST00000278616.8:c.1259_1264del ENSP00000278616.4:p.Ile420_Ser421del
ENST00000278616.9:c.1259_1264del ENSP00000278616.4:p.Ile420_Ser421del
ENST00000452508.6:c.1259_1264del ENSP00000388058.2:p.Ile420_Ser421del
ENST00000452508.7:c.1259_1264del ENSP00000388058.2:p.Ile420_Ser421del
ENST00000527805.5:c.1259_1264del ENSP00000435747.1:p.Ile420_Ser421del
ENST00000527805.6:c.1259_1264del ENSP00000435747.2:p.Ile420_Ser421del
ENST00000675595.1:c.1094_1099del ENSP00000502563.1:p.Ile365_Ser366del
ENST00000682516.1:n.1393_1398del
ENST00000682956.1:n.1393_1398del
ENST00000683174.1:n.1409_1414del
ENST00000683605.1:n.754_759del
ENST00000684037.1:c.*194_*199del ENSP00000508245.1:n.*194_*199del
ENST00000684061.1:n.1393_1398del
ENST00000684179.1:n.1228_1233del
ENST00000713593.1:c.*730_*735del ENSP00000518889.1:n.*730_*735del
XM_005271561.3:c.1259_1264del XP_005271618.2:p.Ile420_Ser421del
XM_005271562.3:c.1259_1264del XP_005271619.2:p.Ile420_Ser421del
XM_005271562.5:c.1259_1264del XP_005271619.2:p.Ile420_Ser421del
XM_006718843.2:c.1259_1264del XP_006718906.1:p.Ile420_Ser421del
XM_006718843.4:c.1259_1264del XP_006718906.1:p.Ile420_Ser421del
XM_011542840.1:c.1259_1264del XP_011541142.1:p.Ile420_Ser421del
XM_011542840.3:c.1259_1264del XP_011541142.1:p.Ile420_Ser421del
XM_011542841.1:c.1259_1264del XP_011541143.1:p.Ile420_Ser421del
XM_011542842.1:c.1094_1099del XP_011541144.1:p.Ile365_Ser366del
XM_011542842.3:c.1094_1099del XP_011541144.1:p.Ile365_Ser366del
XM_011542843.1:c.1259_1264del XP_011541145.1:p.Ile420_Ser421del
XM_011542843.2:c.1259_1264del XP_011541145.1:p.Ile420_Ser421del
XM_011542844.1:c.215_220del XP_011541146.1:p.Ile72_Ser73del
XM_011542844.3:c.215_220del XP_011541146.1:p.Ile72_Ser73del
XM_011542845.1:c.-50_-45del XP_011541147.1:n.-50_-45del
XM_011542845.2:c.-50_-45del XP_011541147.1:n.-50_-45del
XM_011542846.1:c.1259_1264del XP_011541148.1:p.Ile420_Ser421del
XM_017017789.2:c.1259_1264del XP_016873278.1:p.Ile420_Ser421del
XM_017017790.2:c.1259_1264del XP_016873279.1:p.Ile420_Ser421del
XM_017017791.1:c.1259_1264del XP_016873280.1:p.Ile420_Ser421del
XM_017017792.2:c.1259_1264del XP_016873281.1:p.Ile420_Ser421del
XR_002957150.1:n.1992_1997del