Canonical Allele Identifier: CA1998765380

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108245025_108245051delinsAGGTATAAAGGAAATGTTTACTGTTTT , CM000673.2:g.108245025_108245051delinsAGGTATAAAGGAAATGTTTACTGTTTT	GRCh38
NC_000011.9:g.108115752_108115778delinsAGGTATAAAGGAAATGTTTACTGTTTT , CM000673.1:g.108115752_108115778delinsAGGTATAAAGGAAATGTTTACTGTTTT	GRCh37
NC_000011.8:g.107620962_107620988delinsAGGTATAAAGGAAATGTTTACTGTTTT	NCBI36
NG_009830.1:g.27194_27220delinsAGGTATAAAGGAAATGTTTACTGTTTT , LRG_135:g.27194_27220delinsAGGTATAAAGGAAATGTTTACTGTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000713593.1:c.*371_*372+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000278616.9:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000682516.1:n.1034_1035+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000682956.1:n.1034_1035+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000683100.1:n.3247_3248+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000683174.1:n.1050_1051+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000683605.1:n.395_396+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000684037.1:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000684061.1:n.1034_1035+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000684179.1:n.869_870+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000527805.6:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000675595.1:c.735_736+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000675843.1:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000278616.8:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000452508.6:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
ENST00000527805.5:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
NM_000051.3:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT , LRG_135t1:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_005271561.3:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_005271562.3:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_006718843.2:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_011542840.1:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_011542841.1:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_011542842.1:c.735_736+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_011542843.1:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_011542844.1:c.-145_-144+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_011542846.1:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
NM_001351834.1:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_005271562.5:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_006718843.4:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_011542840.3:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_011542842.3:c.735_736+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_011542843.2:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_011542844.3:c.-145_-144+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_017017789.2:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_017017790.2:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_017017791.1:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XM_017017792.2:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
XR_002957150.1:n.1633_1634+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
NM_001351834.2:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT
NM_000051.4:c.900_901+25delinsAGGTATAAAGGAAATGTTTACTGTTTT