Canonical Allele Identifier: CA6264883
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 246258
dbSNP Id: rs771877351

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108252828A>G , CM000673.2:g.108252828A>G GRCh38
NC_000011.9:g.108123555A>G , CM000673.1:g.108123555A>G GRCh37
NC_000011.8:g.107628765A>G NCBI36
NG_009830.1:g.34997A>G , LRG_135:g.34997A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.1814A>G ENSP00000388058.2:p.His605Arg
ENST00000713593.1:c.*1285A>G ENSP00000518889.1:n.*1285A>G
ENST00000278616.9:c.1814A>G ENSP00000278616.4:p.His605Arg
ENST00000682516.1:n.1948A>G
ENST00000683174.1:n.1964A>G
ENST00000683605.1:n.1309A>G
ENST00000684037.1:c.*749A>G ENSP00000508245.1:n.*749A>G
ENST00000684061.1:n.1948A>G
ENST00000527805.6:c.1814A>G ENSP00000435747.2:p.His605Arg
ENST00000675595.1:c.1649A>G ENSP00000502563.1:p.His550Arg
ENST00000675843.1:c.1814A>G MANE Select ENSP00000501606.1:p.His605Arg
ENST00000278616.8:c.1814A>G ENSP00000278616.4:p.His605Arg
ENST00000452508.6:c.1814A>G ENSP00000388058.2:p.His605Arg
ENST00000525012.5:n.8A>G
ENST00000527805.5:c.1814A>G ENSP00000435747.1:p.His605Arg
ENST00000533526.1:n.8A>G
NM_000051.3:c.1814A>G , LRG_135t1:c.1814A>G NP_000042.3:p.His605Arg
XM_005271561.3:c.1814A>G XP_005271618.2:p.His605Arg
XM_005271562.3:c.1814A>G XP_005271619.2:p.His605Arg
XM_006718843.2:c.1814A>G XP_006718906.1:p.His605Arg
XM_011542840.1:c.1814A>G XP_011541142.1:p.His605Arg
XM_011542841.1:c.1814A>G XP_011541143.1:p.His605Arg
XM_011542842.1:c.1649A>G XP_011541144.1:p.His550Arg
XM_011542843.1:c.1814A>G XP_011541145.1:p.His605Arg
XM_011542844.1:c.770A>G XP_011541146.1:p.His257Arg
XM_011542845.1:c.506A>G XP_011541147.1:p.His169Arg
XM_011542846.1:c.1814A>G XP_011541148.1:p.His605Arg
NM_001351834.1:c.1814A>G NP_001338763.1:p.His605Arg
XM_005271562.5:c.1814A>G XP_005271619.2:p.His605Arg
XM_006718843.4:c.1814A>G XP_006718906.1:p.His605Arg
XM_011542840.3:c.1814A>G XP_011541142.1:p.His605Arg
XM_011542842.3:c.1649A>G XP_011541144.1:p.His550Arg
XM_011542843.2:c.1814A>G XP_011541145.1:p.His605Arg
XM_011542844.3:c.770A>G XP_011541146.1:p.His257Arg
XM_011542845.2:c.506A>G XP_011541147.1:p.His169Arg
XM_017017789.2:c.1814A>G XP_016873278.1:p.His605Arg
XM_017017790.2:c.1814A>G XP_016873279.1:p.His605Arg
XM_017017791.1:c.1814A>G XP_016873280.1:p.His605Arg
XM_017017792.2:c.1814A>G XP_016873281.1:p.His605Arg
XR_002957150.1:n.2547A>G
NM_001351834.2:c.1814A>G NP_001338763.1:p.His605Arg
NM_000051.4:c.1814A>G MANE Select NP_000042.3:p.His605Arg