Canonical Allele Identifier: CA228367897
Gene: ATM HGNC NCBI

Linked Data

dbSNP Id: rs765514838

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108284142_108284147del , CM000673.2:g.108284142_108284147del GRCh38
NC_000011.9:g.108154869_108154874del , CM000673.1:g.108154869_108154874del GRCh37
NC_000011.8:g.107660079_107660084del NCBI36
NG_009830.1:g.66311_66316del , LRG_135:g.66311_66316del

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.3747-85_3747-80del ENSP00000388058.2:n.3747-85_3747-80del
ENST00000713593.1:c.*3218-85_*3218-80del ENSP00000518889.1:n.*3218-85_*3218-80del
ENST00000278616.9:c.3747-85_3747-80del ENSP00000278616.4:n.3747-85_3747-80del
ENST00000682289.1:n.94-85_94-80del
ENST00000683174.1:n.3897-85_3897-80del
ENST00000527805.6:c.3747-85_3747-80del ENSP00000435747.2:n.3747-85_3747-80del
ENST00000675595.1:c.3582-85_3582-80del ENSP00000502563.1:n.3582-85_3582-80del
ENST00000675843.1:c.3747-85_3747-80del MANE Select ENSP00000501606.1:n.3747-85_3747-80del
ENST00000278616.8:c.3747-85_3747-80del ENSP00000278616.4:n.3747-85_3747-80del
ENST00000452508.6:c.3747-85_3747-80del ENSP00000388058.2:n.3747-85_3747-80del
ENST00000527805.5:c.3747-85_3747-80del ENSP00000435747.1:n.3747-85_3747-80del
NM_000051.3:c.3747-85_3747-80del , LRG_135t1:c.3747-85_3747-80del NP_000042.3:n.3747-85_3747-80del
XM_005271561.3:c.3747-85_3747-80del XP_005271618.2:n.3747-85_3747-80del
XM_005271562.3:c.3747-85_3747-80del XP_005271619.2:n.3747-85_3747-80del
XM_006718843.2:c.3747-85_3747-80del XP_006718906.1:n.3747-85_3747-80del
XM_011542840.1:c.3747-85_3747-80del XP_011541142.1:n.3747-85_3747-80del
XM_011542841.1:c.3747-85_3747-80del XP_011541143.1:n.3747-85_3747-80del
XM_011542842.1:c.3582-85_3582-80del XP_011541144.1:n.3582-85_3582-80del
XM_011542843.1:c.3747-85_3747-80del XP_011541145.1:n.3747-85_3747-80del
XM_011542844.1:c.2703-85_2703-80del XP_011541146.1:n.2703-85_2703-80del
XM_011542845.1:c.2439-85_2439-80del XP_011541147.1:n.2439-85_2439-80del
XM_011542846.1:c.3747-85_3747-80del XP_011541148.1:n.3747-85_3747-80del
NM_001351834.1:c.3747-85_3747-80del NP_001338763.1:n.3747-85_3747-80del
XM_005271562.5:c.3747-85_3747-80del XP_005271619.2:n.3747-85_3747-80del
XM_006718843.4:c.3747-85_3747-80del XP_006718906.1:n.3747-85_3747-80del
XM_011542840.3:c.3747-85_3747-80del XP_011541142.1:n.3747-85_3747-80del
XM_011542842.3:c.3582-85_3582-80del XP_011541144.1:n.3582-85_3582-80del
XM_011542843.2:c.3747-85_3747-80del XP_011541145.1:n.3747-85_3747-80del
XM_011542844.3:c.2703-85_2703-80del XP_011541146.1:n.2703-85_2703-80del
XM_011542845.2:c.2439-85_2439-80del XP_011541147.1:n.2439-85_2439-80del
XM_017017789.2:c.3747-85_3747-80del XP_016873278.1:n.3747-85_3747-80del
XM_017017790.2:c.3747-85_3747-80del XP_016873279.1:n.3747-85_3747-80del
XM_017017791.1:c.3747-85_3747-80del XP_016873280.1:n.3747-85_3747-80del
XM_017017792.2:c.3747-85_3747-80del XP_016873281.1:n.3747-85_3747-80del
XR_002957150.1:n.4480-85_4480-80del
NM_001351834.2:c.3747-85_3747-80del NP_001338763.1:n.3747-85_3747-80del
NM_000051.4:c.3747-85_3747-80del MANE Select NP_000042.3:n.3747-85_3747-80del