Canonical Allele Identifier: CA1998784665
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108289526_108289527delinsGA , CM000673.2:g.108289526_108289527delinsGA GRCh38
NC_000011.9:g.108160253_108160254delinsGA , CM000673.1:g.108160253_108160254delinsGA GRCh37
NC_000011.8:g.107665463_107665464delinsGA NCBI36
NG_009830.1:g.71695_71696delinsGA , LRG_135:g.71695_71696delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.4237-76_4237-75delinsGA ENSP00000388058.2:n.4237-76_4237-75delins...
ENST00000713593.1:c.*3708-76_*3708-75delinsGA ENSP00000518889.1:n.*3708-76_*3708-75deli...
ENST00000278616.9:c.4237-76_4237-75delinsGA ENSP00000278616.4:n.4237-76_4237-75delins...
ENST00000533733.6:n.1500-76_1500-75delinsGA
ENST00000683174.1:n.4387-76_4387-75delinsGA
ENST00000527805.6:c.4237-76_4237-75delinsGA ENSP00000435747.2:n.4237-76_4237-75delins...
ENST00000675595.1:c.4072-76_4072-75delinsGA ENSP00000502563.1:n.4072-76_4072-75delins...
ENST00000675843.1:c.4237-76_4237-75delinsGA MANE Select ENSP00000501606.1:n.4237-76_4237-75delins...
ENST00000278616.8:c.4237-76_4237-75delinsGA ENSP00000278616.4:n.4237-76_4237-75delins...
ENST00000452508.6:c.4237-76_4237-75delinsGA ENSP00000388058.2:n.4237-76_4237-75delins...
ENST00000524792.5:n.452-76_452-75delinsGA
ENST00000531525.2:c.244-76_244-75delinsGA ENSP00000434327.2:n.244-76_244-75delinsGA...
ENST00000533733.5:n.666-76_666-75delinsGA
NM_000051.3:c.4237-76_4237-75delinsGA , LRG_135t1:c.4237-76_4237-75delinsGA NP_000042.3:n.4237-76_4237-75delinsGA
XM_005271561.3:c.4237-76_4237-75delinsGA XP_005271618.2:n.4237-76_4237-75delinsGA
XM_005271562.3:c.4237-76_4237-75delinsGA XP_005271619.2:n.4237-76_4237-75delinsGA
XM_006718843.2:c.4237-76_4237-75delinsGA XP_006718906.1:n.4237-76_4237-75delinsGA
XM_006718845.1:c.193-76_193-75delinsGA XP_006718908.1:n.193-76_193-75delinsGA
XM_011542840.1:c.4237-76_4237-75delinsGA XP_011541142.1:n.4237-76_4237-75delinsGA
XM_011542841.1:c.4237-76_4237-75delinsGA XP_011541143.1:n.4237-76_4237-75delinsGA
XM_011542842.1:c.4072-76_4072-75delinsGA XP_011541144.1:n.4072-76_4072-75delinsGA
XM_011542843.1:c.4237-76_4237-75delinsGA XP_011541145.1:n.4237-76_4237-75delinsGA
XM_011542844.1:c.3193-76_3193-75delinsGA XP_011541146.1:n.3193-76_3193-75delinsGA
XM_011542845.1:c.2929-76_2929-75delinsGA XP_011541147.1:n.2929-76_2929-75delinsGA
XM_011542846.1:c.4237-76_4237-75delinsGA XP_011541148.1:n.4237-76_4237-75delinsGA
NM_001351834.1:c.4237-76_4237-75delinsGA NP_001338763.1:n.4237-76_4237-75delinsGA
XM_005271562.5:c.4237-76_4237-75delinsGA XP_005271619.2:n.4237-76_4237-75delinsGA
XM_006718843.4:c.4237-76_4237-75delinsGA XP_006718906.1:n.4237-76_4237-75delinsGA
XM_006718845.2:c.193-76_193-75delinsGA XP_006718908.1:n.193-76_193-75delinsGA
XM_011542840.3:c.4237-76_4237-75delinsGA XP_011541142.1:n.4237-76_4237-75delinsGA
XM_011542842.3:c.4072-76_4072-75delinsGA XP_011541144.1:n.4072-76_4072-75delinsGA
XM_011542843.2:c.4237-76_4237-75delinsGA XP_011541145.1:n.4237-76_4237-75delinsGA
XM_011542844.3:c.3193-76_3193-75delinsGA XP_011541146.1:n.3193-76_3193-75delinsGA
XM_011542845.2:c.2929-76_2929-75delinsGA XP_011541147.1:n.2929-76_2929-75delinsGA
XM_017017789.2:c.4237-76_4237-75delinsGA XP_016873278.1:n.4237-76_4237-75delinsGA
XM_017017790.2:c.4237-76_4237-75delinsGA XP_016873279.1:n.4237-76_4237-75delinsGA
XM_017017791.1:c.4237-76_4237-75delinsGA XP_016873280.1:n.4237-76_4237-75delinsGA
XM_017017792.2:c.4237-76_4237-75delinsGA XP_016873281.1:n.4237-76_4237-75delinsGA
XR_002957150.1:n.4970-76_4970-75delinsGA
NM_001351834.2:c.4237-76_4237-75delinsGA NP_001338763.1:n.4237-76_4237-75delinsGA
NM_000051.4:c.4237-76_4237-75delinsGA MANE Select NP_000042.3:n.4237-76_4237-75delinsGA