Canonical Allele Identifier: CA2739291534
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108299751dup , CM000673.2:g.108299751dup GRCh38
NC_000011.9:g.108170478dup , CM000673.1:g.108170478dup GRCh37
NC_000011.8:g.107675688dup NCBI36
NG_009830.1:g.81920dup , LRG_135:g.81920dup

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.5043dup ENSP00000388058.2:p.Asp1682ArgfsTer10
ENST00000713593.1:c.*4514dup ENSP00000518889.1:n.*4514dup
ENST00000278616.9:c.5043dup ENSP00000278616.4:p.Asp1682ArgfsTer10
ENST00000683174.1:n.6527dup
ENST00000683524.1:n.267dup
ENST00000684152.1:n.757dup
ENST00000527805.6:c.*107dup ENSP00000435747.2:n.*107dup
ENST00000675595.1:c.*107dup ENSP00000502563.1:n.*107dup
ENST00000675843.1:c.5043dup MANE Select ENSP00000501606.1:p.Asp1682ArgfsTer10
ENST00000278616.8:c.5043dup ENSP00000278616.4:p.Asp1682ArgfsTer10
ENST00000452508.6:c.5043dup ENSP00000388058.2:p.Asp1682ArgfsTer10
ENST00000524792.5:n.1258dup
ENST00000533690.5:n.447dup
ENST00000534625.1:n.272dup
NM_000051.3:c.5043dup , LRG_135t1:c.5043dup NP_000042.3:p.Asp1682ArgfsTer10
XM_005271561.3:c.5043dup XP_005271618.2:p.Asp1682ArgfsTer10
XM_005271562.3:c.5043dup XP_005271619.2:p.Asp1682ArgfsTer10
XM_006718843.2:c.5043dup XP_006718906.1:p.Asp1682ArgfsTer10
XM_006718845.1:c.999dup XP_006718908.1:p.Asp334ArgfsTer10
XM_011542840.1:c.5043dup XP_011541142.1:p.Asp1682ArgfsTer10
XM_011542841.1:c.5043dup XP_011541143.1:p.Asp1682ArgfsTer10
XM_011542842.1:c.4878dup XP_011541144.1:p.Asp1627ArgfsTer10
XM_011542843.1:c.5043dup XP_011541145.1:p.Asp1682ArgfsTer10
XM_011542844.1:c.3999dup XP_011541146.1:p.Asp1334ArgfsTer10
XM_011542845.1:c.3735dup XP_011541147.1:p.Asp1246ArgfsTer10
XM_011542846.1:c.5043dup XP_011541148.1:p.Asp1682ArgfsTer10
XM_011542847.1:c.114dup XP_011541149.1:p.Asp39ArgfsTer10
NM_001351834.1:c.5043dup NP_001338763.1:p.Asp1682ArgfsTer10
XM_005271562.5:c.5043dup XP_005271619.2:p.Asp1682ArgfsTer10
XM_006718843.4:c.5043dup XP_006718906.1:p.Asp1682ArgfsTer10
XM_006718845.2:c.999dup XP_006718908.1:p.Asp334ArgfsTer10
XM_011542840.3:c.5043dup XP_011541142.1:p.Asp1682ArgfsTer10
XM_011542842.3:c.4878dup XP_011541144.1:p.Asp1627ArgfsTer10
XM_011542843.2:c.5043dup XP_011541145.1:p.Asp1682ArgfsTer10
XM_011542844.3:c.3999dup XP_011541146.1:p.Asp1334ArgfsTer10
XM_011542845.2:c.3735dup XP_011541147.1:p.Asp1246ArgfsTer10
XM_017017789.2:c.5043dup XP_016873278.1:p.Asp1682ArgfsTer10
XM_017017790.2:c.5043dup XP_016873279.1:p.Asp1682ArgfsTer10
XM_017017791.1:c.5043dup XP_016873280.1:p.Asp1682ArgfsTer10
XM_017017792.2:c.5043dup XP_016873281.1:p.Asp1682ArgfsTer10
XR_002957150.1:n.5643dup
NM_001351834.2:c.5043dup NP_001338763.1:p.Asp1682ArgfsTer10
NM_000051.4:c.5043dup MANE Select NP_000042.3:p.Asp1682ArgfsTer10