Canonical Allele Identifier: CA197891
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187534
ClinVar RCV Id: RCV000167269
dbSNP Id: rs786203807

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108256219del , CM000673.2:g.108256219del GRCh38
NC_000011.9:g.108126946del , CM000673.1:g.108126946del GRCh37
NC_000011.8:g.107632156del NCBI36
NG_009830.1:g.38388del , LRG_135:g.38388del

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.2129del ENSP00000388058.2:p.Thr710LysfsTer25
ENST00000713593.1:c.*1600del ENSP00000518889.1:n.*1600del
ENST00000278616.9:c.2129del ENSP00000278616.4:p.Thr710LysfsTer25
ENST00000682516.1:n.2263del
ENST00000683174.1:n.2279del
ENST00000683605.1:n.1624del
ENST00000684037.1:c.*1064del ENSP00000508245.1:n.*1064del
ENST00000684061.1:n.2263del
ENST00000527805.6:c.2129del ENSP00000435747.2:p.Thr710LysfsTer25
ENST00000675595.1:c.1964del ENSP00000502563.1:p.Thr655LysfsTer25
ENST00000675843.1:c.2129del MANE Select ENSP00000501606.1:p.Thr710LysfsTer25
ENST00000278616.8:c.2129del ENSP00000278616.4:p.Thr710LysfsTer25
ENST00000452508.6:c.2129del ENSP00000388058.2:p.Thr710LysfsTer25
ENST00000527805.5:c.2129del ENSP00000435747.1:p.Thr710LysfsTer25
NM_000051.3:c.2129del , LRG_135t1:c.2129del NP_000042.3:p.Thr710LysfsTer25
XM_005271561.3:c.2129del XP_005271618.2:p.Thr710LysfsTer25
XM_005271562.3:c.2129del XP_005271619.2:p.Thr710LysfsTer25
XM_006718843.2:c.2129del XP_006718906.1:p.Thr710LysfsTer25
XM_011542840.1:c.2129del XP_011541142.1:p.Thr710LysfsTer25
XM_011542841.1:c.2129del XP_011541143.1:p.Thr710LysfsTer25
XM_011542842.1:c.1964del XP_011541144.1:p.Thr655LysfsTer25
XM_011542843.1:c.2129del XP_011541145.1:p.Thr710LysfsTer25
XM_011542844.1:c.1085del XP_011541146.1:p.Thr362LysfsTer25
XM_011542845.1:c.821del XP_011541147.1:p.Thr274LysfsTer25
XM_011542846.1:c.2129del XP_011541148.1:p.Thr710LysfsTer25
NM_001351834.1:c.2129del NP_001338763.1:p.Thr710LysfsTer25
XM_005271562.5:c.2129del XP_005271619.2:p.Thr710LysfsTer25
XM_006718843.4:c.2129del XP_006718906.1:p.Thr710LysfsTer25
XM_011542840.3:c.2129del XP_011541142.1:p.Thr710LysfsTer25
XM_011542842.3:c.1964del XP_011541144.1:p.Thr655LysfsTer25
XM_011542843.2:c.2129del XP_011541145.1:p.Thr710LysfsTer25
XM_011542844.3:c.1085del XP_011541146.1:p.Thr362LysfsTer25
XM_011542845.2:c.821del XP_011541147.1:p.Thr274LysfsTer25
XM_017017789.2:c.2129del XP_016873278.1:p.Thr710LysfsTer25
XM_017017790.2:c.2129del XP_016873279.1:p.Thr710LysfsTer25
XM_017017791.1:c.2129del XP_016873280.1:p.Thr710LysfsTer25
XM_017017792.2:c.2129del XP_016873281.1:p.Thr710LysfsTer25
XR_002957150.1:n.2862del
NM_001351834.2:c.2129del NP_001338763.1:p.Thr710LysfsTer25
NM_000051.4:c.2129del MANE Select NP_000042.3:p.Thr710LysfsTer25