Canonical Allele Identifier: CA891842902
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 583404
ClinVar RCV Id: RCV000707730
dbSNP Id: rs1565375055

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108247009_108247013del , CM000673.2:g.108247009_108247013del GRCh38
NC_000011.9:g.108117736_108117740del , CM000673.1:g.108117736_108117740del GRCh37
NC_000011.8:g.107622946_107622950del NCBI36
NG_009830.1:g.29178_29182del , LRG_135:g.29178_29182del

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.947_951del ENSP00000388058.2:p.Tyr316SerfsTer5
ENST00000713593.1:c.*418_*422del ENSP00000518889.1:n.*418_*422del
ENST00000278616.9:c.947_951del ENSP00000278616.4:p.Tyr316SerfsTer5
ENST00000682516.1:n.1081_1085del
ENST00000682956.1:n.1081_1085del
ENST00000683100.1:n.3294_3298del
ENST00000683174.1:n.1097_1101del
ENST00000683605.1:n.442_446del
ENST00000684037.1:c.947_951del ENSP00000508245.1:p.Tyr316SerfsTer5
ENST00000684061.1:n.1081_1085del
ENST00000684179.1:n.916_920del
ENST00000527805.6:c.947_951del ENSP00000435747.2:p.Tyr316SerfsTer5
ENST00000675595.1:c.782_786del ENSP00000502563.1:p.Tyr261SerfsTer5
ENST00000675843.1:c.947_951del MANE Select ENSP00000501606.1:p.Tyr316SerfsTer5
ENST00000278616.8:c.947_951del ENSP00000278616.4:p.Tyr316SerfsTer5
ENST00000452508.6:c.947_951del ENSP00000388058.2:p.Tyr316SerfsTer5
ENST00000527805.5:c.947_951del ENSP00000435747.1:p.Tyr316SerfsTer5
NM_000051.3:c.947_951del , LRG_135t1:c.947_951del NP_000042.3:p.Tyr316SerfsTer5
XM_005271561.3:c.947_951del XP_005271618.2:p.Tyr316SerfsTer5
XM_005271562.3:c.947_951del XP_005271619.2:p.Tyr316SerfsTer5
XM_006718843.2:c.947_951del XP_006718906.1:p.Tyr316SerfsTer5
XM_011542840.1:c.947_951del XP_011541142.1:p.Tyr316SerfsTer5
XM_011542841.1:c.947_951del XP_011541143.1:p.Tyr316SerfsTer5
XM_011542842.1:c.782_786del XP_011541144.1:p.Tyr261SerfsTer5
XM_011542843.1:c.947_951del XP_011541145.1:p.Tyr316SerfsTer5
XM_011542844.1:c.-98_-94del XP_011541146.1:n.-98_-94del
XM_011542846.1:c.947_951del XP_011541148.1:p.Tyr316SerfsTer5
NM_001351834.1:c.947_951del NP_001338763.1:p.Tyr316SerfsTer5
XM_005271562.5:c.947_951del XP_005271619.2:p.Tyr316SerfsTer5
XM_006718843.4:c.947_951del XP_006718906.1:p.Tyr316SerfsTer5
XM_011542840.3:c.947_951del XP_011541142.1:p.Tyr316SerfsTer5
XM_011542842.3:c.782_786del XP_011541144.1:p.Tyr261SerfsTer5
XM_011542843.2:c.947_951del XP_011541145.1:p.Tyr316SerfsTer5
XM_011542844.3:c.-98_-94del XP_011541146.1:n.-98_-94del
XM_017017789.2:c.947_951del XP_016873278.1:p.Tyr316SerfsTer5
XM_017017790.2:c.947_951del XP_016873279.1:p.Tyr316SerfsTer5
XM_017017791.1:c.947_951del XP_016873280.1:p.Tyr316SerfsTer5
XM_017017792.2:c.947_951del XP_016873281.1:p.Tyr316SerfsTer5
XR_002957150.1:n.1680_1684del
NM_001351834.2:c.947_951del NP_001338763.1:p.Tyr316SerfsTer5
NM_000051.4:c.947_951del MANE Select NP_000042.3:p.Tyr316SerfsTer5