Canonical Allele Identifier: CA2725190665
Gene: ATM HGNC NCBI

Linked Data

dbSNP Id: rs2135706485

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108284320_108284323del , CM000673.2:g.108284320_108284323del GRCh38
NC_000011.9:g.108155047_108155050del , CM000673.1:g.108155047_108155050del GRCh37
NC_000011.8:g.107660257_107660260del NCBI36
NG_009830.1:g.66489_66492del , LRG_135:g.66489_66492del

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.3840_3843del ENSP00000388058.2:p.Lys1280AsnfsTer3
ENST00000713593.1:c.*3311_*3314del ENSP00000518889.1:n.*3311_*3314del
ENST00000278616.9:c.3840_3843del ENSP00000278616.4:p.Lys1280AsnfsTer3
ENST00000682289.1:n.187_190del
ENST00000683174.1:n.3990_3993del
ENST00000527805.6:c.3840_3843del ENSP00000435747.2:p.Lys1280AsnfsTer3
ENST00000675595.1:c.3675_3678del ENSP00000502563.1:p.Lys1225AsnfsTer3
ENST00000675843.1:c.3840_3843del MANE Select ENSP00000501606.1:p.Lys1280AsnfsTer3
ENST00000278616.8:c.3840_3843del ENSP00000278616.4:p.Lys1280AsnfsTer3
ENST00000452508.6:c.3840_3843del ENSP00000388058.2:p.Lys1280AsnfsTer3
ENST00000527805.5:c.3840_3843del ENSP00000435747.1:p.Lys1280AsnfsTer3
NM_000051.3:c.3840_3843del , LRG_135t1:c.3840_3843del NP_000042.3:p.Lys1280AsnfsTer3
XM_005271561.3:c.3840_3843del XP_005271618.2:p.Lys1280AsnfsTer3
XM_005271562.3:c.3840_3843del XP_005271619.2:p.Lys1280AsnfsTer3
XM_006718843.2:c.3840_3843del XP_006718906.1:p.Lys1280AsnfsTer3
XM_011542840.1:c.3840_3843del XP_011541142.1:p.Lys1280AsnfsTer3
XM_011542841.1:c.3840_3843del XP_011541143.1:p.Lys1280AsnfsTer3
XM_011542842.1:c.3675_3678del XP_011541144.1:p.Lys1225AsnfsTer3
XM_011542843.1:c.3840_3843del XP_011541145.1:p.Lys1280AsnfsTer3
XM_011542844.1:c.2796_2799del XP_011541146.1:p.Lys932AsnfsTer3
XM_011542845.1:c.2532_2535del XP_011541147.1:p.Lys844AsnfsTer3
XM_011542846.1:c.3840_3843del XP_011541148.1:p.Lys1280AsnfsTer3
NM_001351834.1:c.3840_3843del NP_001338763.1:p.Lys1280AsnfsTer3
XM_005271562.5:c.3840_3843del XP_005271619.2:p.Lys1280AsnfsTer3
XM_006718843.4:c.3840_3843del XP_006718906.1:p.Lys1280AsnfsTer3
XM_011542840.3:c.3840_3843del XP_011541142.1:p.Lys1280AsnfsTer3
XM_011542842.3:c.3675_3678del XP_011541144.1:p.Lys1225AsnfsTer3
XM_011542843.2:c.3840_3843del XP_011541145.1:p.Lys1280AsnfsTer3
XM_011542844.3:c.2796_2799del XP_011541146.1:p.Lys932AsnfsTer3
XM_011542845.2:c.2532_2535del XP_011541147.1:p.Lys844AsnfsTer3
XM_017017789.2:c.3840_3843del XP_016873278.1:p.Lys1280AsnfsTer3
XM_017017790.2:c.3840_3843del XP_016873279.1:p.Lys1280AsnfsTer3
XM_017017791.1:c.3840_3843del XP_016873280.1:p.Lys1280AsnfsTer3
XM_017017792.2:c.3840_3843del XP_016873281.1:p.Lys1280AsnfsTer3
XR_002957150.1:n.4573_4576del
NM_001351834.2:c.3840_3843del NP_001338763.1:p.Lys1280AsnfsTer3
NM_000051.4:c.3840_3843del MANE Select NP_000042.3:p.Lys1280AsnfsTer3