Canonical Allele Identifier: CA16613131
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407679
ClinVar RCV Id: RCV003233640
dbSNP Id: rs1060501676

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108281042_108281046del , CM000673.2:g.108281042_108281046del GRCh38
NC_000011.9:g.108151769_108151773del , CM000673.1:g.108151769_108151773del GRCh37
NC_000011.8:g.107656979_107656983del NCBI36
NG_009830.1:g.63211_63215del , LRG_135:g.63211_63215del

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.3450_3454del ENSP00000388058.2:p.Arg1150SerfsTer14
ENST00000713593.1:c.*2921_*2925del ENSP00000518889.1:n.*2921_*2925del
ENST00000278616.9:c.3450_3454del ENSP00000278616.4:p.Arg1150SerfsTer14
ENST00000683174.1:n.3600_3604del
ENST00000527805.6:c.3450_3454del ENSP00000435747.2:p.Arg1150SerfsTer14
ENST00000675595.1:c.3285_3289del ENSP00000502563.1:p.Arg1095SerfsTer14
ENST00000675843.1:c.3450_3454del MANE Select ENSP00000501606.1:p.Arg1150SerfsTer14
ENST00000278616.8:c.3450_3454del ENSP00000278616.4:p.Arg1150SerfsTer14
ENST00000452508.6:c.3450_3454del ENSP00000388058.2:p.Arg1150SerfsTer14
ENST00000527805.5:c.3450_3454del ENSP00000435747.1:p.Arg1150SerfsTer14
NM_000051.3:c.3450_3454del , LRG_135t1:c.3450_3454del NP_000042.3:p.Arg1150SerfsTer14
XM_005271561.3:c.3450_3454del XP_005271618.2:p.Arg1150SerfsTer14
XM_005271562.3:c.3450_3454del XP_005271619.2:p.Arg1150SerfsTer14
XM_006718843.2:c.3450_3454del XP_006718906.1:p.Arg1150SerfsTer14
XM_011542840.1:c.3450_3454del XP_011541142.1:p.Arg1150SerfsTer14
XM_011542841.1:c.3450_3454del XP_011541143.1:p.Arg1150SerfsTer14
XM_011542842.1:c.3285_3289del XP_011541144.1:p.Arg1095SerfsTer14
XM_011542843.1:c.3450_3454del XP_011541145.1:p.Arg1150SerfsTer14
XM_011542844.1:c.2406_2410del XP_011541146.1:p.Arg802SerfsTer14
XM_011542845.1:c.2142_2146del XP_011541147.1:p.Arg714SerfsTer14
XM_011542846.1:c.3450_3454del XP_011541148.1:p.Arg1150SerfsTer14
NM_001351834.1:c.3450_3454del NP_001338763.1:p.Arg1150SerfsTer14
XM_005271562.5:c.3450_3454del XP_005271619.2:p.Arg1150SerfsTer14
XM_006718843.4:c.3450_3454del XP_006718906.1:p.Arg1150SerfsTer14
XM_011542840.3:c.3450_3454del XP_011541142.1:p.Arg1150SerfsTer14
XM_011542842.3:c.3285_3289del XP_011541144.1:p.Arg1095SerfsTer14
XM_011542843.2:c.3450_3454del XP_011541145.1:p.Arg1150SerfsTer14
XM_011542844.3:c.2406_2410del XP_011541146.1:p.Arg802SerfsTer14
XM_011542845.2:c.2142_2146del XP_011541147.1:p.Arg714SerfsTer14
XM_017017789.2:c.3450_3454del XP_016873278.1:p.Arg1150SerfsTer14
XM_017017790.2:c.3450_3454del XP_016873279.1:p.Arg1150SerfsTer14
XM_017017791.1:c.3450_3454del XP_016873280.1:p.Arg1150SerfsTer14
XM_017017792.2:c.3450_3454del XP_016873281.1:p.Arg1150SerfsTer14
XR_002957150.1:n.4183_4187del
NM_001351834.2:c.3450_3454del NP_001338763.1:p.Arg1150SerfsTer14
NM_000051.4:c.3450_3454del MANE Select NP_000042.3:p.Arg1150SerfsTer14