Canonical Allele Identifier: CA298012
Gene: ATM HGNC NCBI

Linked Data

dbSNP Id: rs730881298

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108258971_108258974del , CM000673.2:g.108258971_108258974del GRCh38
NC_000011.9:g.108129698_108129701del , CM000673.1:g.108129698_108129701del GRCh37
NC_000011.8:g.107634908_107634911del NCBI36
NG_009830.1:g.41140_41143del , LRG_135:g.41140_41143del

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.2377-15_2377-12del ENSP00000388058.2:n.2377-15_2377-12del
ENST00000713593.1:c.*1848-15_*1848-12del ENSP00000518889.1:n.*1848-15_*1848-12del
ENST00000278616.9:c.2377-15_2377-12del ENSP00000278616.4:n.2377-15_2377-12del
ENST00000682516.1:n.2511-15_2511-12del
ENST00000683174.1:n.2527-15_2527-12del
ENST00000683605.1:n.1872-15_1872-12del
ENST00000684037.1:c.*1312-15_*1312-12del ENSP00000508245.1:n.*1312-15_*1312-12del
ENST00000527805.6:c.2377-15_2377-12del ENSP00000435747.2:n.2377-15_2377-12del
ENST00000675595.1:c.2212-15_2212-12del ENSP00000502563.1:n.2212-15_2212-12del
ENST00000675843.1:c.2377-15_2377-12del MANE Select ENSP00000501606.1:n.2377-15_2377-12del
ENST00000278616.8:c.2377-15_2377-12del ENSP00000278616.4:n.2377-15_2377-12del
ENST00000452508.6:c.2377-15_2377-12del ENSP00000388058.2:n.2377-15_2377-12del
ENST00000527805.5:c.2377-15_2377-12del ENSP00000435747.1:n.2377-15_2377-12del
NM_000051.3:c.2377-15_2377-12del , LRG_135t1:c.2377-15_2377-12del NP_000042.3:n.2377-15_2377-12del
XM_005271561.3:c.2377-15_2377-12del XP_005271618.2:n.2377-15_2377-12del
XM_005271562.3:c.2377-15_2377-12del XP_005271619.2:n.2377-15_2377-12del
XM_006718843.2:c.2377-15_2377-12del XP_006718906.1:n.2377-15_2377-12del
XM_011542840.1:c.2377-15_2377-12del XP_011541142.1:n.2377-15_2377-12del
XM_011542841.1:c.2377-15_2377-12del XP_011541143.1:n.2377-15_2377-12del
XM_011542842.1:c.2212-15_2212-12del XP_011541144.1:n.2212-15_2212-12del
XM_011542843.1:c.2377-15_2377-12del XP_011541145.1:n.2377-15_2377-12del
XM_011542844.1:c.1333-15_1333-12del XP_011541146.1:n.1333-15_1333-12del
XM_011542845.1:c.1069-15_1069-12del XP_011541147.1:n.1069-15_1069-12del
XM_011542846.1:c.2377-15_2377-12del XP_011541148.1:n.2377-15_2377-12del
NM_001351834.1:c.2377-15_2377-12del NP_001338763.1:n.2377-15_2377-12del
XM_005271562.5:c.2377-15_2377-12del XP_005271619.2:n.2377-15_2377-12del
XM_006718843.4:c.2377-15_2377-12del XP_006718906.1:n.2377-15_2377-12del
XM_011542840.3:c.2377-15_2377-12del XP_011541142.1:n.2377-15_2377-12del
XM_011542842.3:c.2212-15_2212-12del XP_011541144.1:n.2212-15_2212-12del
XM_011542843.2:c.2377-15_2377-12del XP_011541145.1:n.2377-15_2377-12del
XM_011542844.3:c.1333-15_1333-12del XP_011541146.1:n.1333-15_1333-12del
XM_011542845.2:c.1069-15_1069-12del XP_011541147.1:n.1069-15_1069-12del
XM_017017789.2:c.2377-15_2377-12del XP_016873278.1:n.2377-15_2377-12del
XM_017017790.2:c.2377-15_2377-12del XP_016873279.1:n.2377-15_2377-12del
XM_017017791.1:c.2377-15_2377-12del XP_016873280.1:n.2377-15_2377-12del
XM_017017792.2:c.2377-15_2377-12del XP_016873281.1:n.2377-15_2377-12del
XR_002957150.1:n.3110-15_3110-12del
NM_001351834.2:c.2377-15_2377-12del NP_001338763.1:n.2377-15_2377-12del
NM_000051.4:c.2377-15_2377-12del MANE Select NP_000042.3:n.2377-15_2377-12del