Canonical Allele Identifier: CA228364248
Gene: ATM HGNC NCBI

Linked Data

dbSNP Id: rs963921655

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108222936_108222937del , CM000673.2:g.108222936_108222937del GRCh38
NC_000011.9:g.108093663_108093664del , CM000673.1:g.108093663_108093664del GRCh37
NC_000011.8:g.107598873_107598874del NCBI36
NG_009830.1:g.5105_5106del , LRG_135:g.5105_5106del

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.-369_-368del ENSP00000388058.2:n.-369_-368del
ENST00000683914.2:c.-281_-280del ENSP00000507649.1:n.-281_-280del
ENST00000278616.8:c.-281_-280del ENSP00000278616.4:n.-281_-280del
ENST00000527805.5:c.-281_-280del ENSP00000435747.1:n.-281_-280del
NM_000051.3:c.-281_-280del , LRG_135t1:c.-281_-280del NP_000042.3:n.-281_-280del
XM_011542843.1:c.-281_-280del XP_011541145.1:n.-281_-280del
XM_011542846.1:c.-281_-280del XP_011541148.1:n.-281_-280del
NM_001351834.1:c.-369_-368del NP_001338763.1:n.-369_-368del
NM_001351835.1:c.-281_-280del NP_001338764.1:n.-281_-280del
XM_011542842.3:c.-281_-280del XP_011541144.1:n.-281_-280del
XM_011542843.2:c.-281_-280del XP_011541145.1:n.-281_-280del
XM_011542844.3:c.-1303_-1302del XP_011541146.1:n.-1303_-1302del
XM_017017791.1:c.-281_-280del XP_016873280.1:n.-281_-280del
XM_017017792.2:c.-281_-280del XP_016873281.1:n.-281_-280del
XR_002957150.1:n.453_454del