Canonical Allele Identifier: CA2695214768
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108288977_108289029del , CM000673.2:g.108288977_108289029del GRCh38
NC_000011.9:g.108159704_108159756del , CM000673.1:g.108159704_108159756del GRCh37
NC_000011.8:g.107664914_107664966del NCBI36
NG_009830.1:g.71146_71198del , LRG_135:g.71146_71198del

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.4110_4162del
ENST00000713593.1:c.*3581_*3633del
ENST00000278616.9:c.4110_4162del
ENST00000533733.6:n.1373_1425del
ENST00000683174.1:n.4260_4312del
ENST00000527805.6:c.4110_4162del
ENST00000675595.1:c.3945_3997del
ENST00000675843.1:c.4110_4162del
ENST00000278616.8:c.4110_4162del
ENST00000452508.6:c.4110_4162del
ENST00000524792.5:n.325_377del
ENST00000531525.2:c.117_169del
ENST00000533733.5:n.539_591del
NM_000051.3:c.4110_4162del , LRG_135t1:c.4110_4162del
XM_005271561.3:c.4110_4162del
XM_005271562.3:c.4110_4162del
XM_006718843.2:c.4110_4162del
XM_006718845.1:c.66_118del
XM_011542840.1:c.4110_4162del
XM_011542841.1:c.4110_4162del
XM_011542842.1:c.3945_3997del
XM_011542843.1:c.4110_4162del
XM_011542844.1:c.3066_3118del
XM_011542845.1:c.2802_2854del
XM_011542846.1:c.4110_4162del
NM_001351834.1:c.4110_4162del
XM_005271562.5:c.4110_4162del
XM_006718843.4:c.4110_4162del
XM_006718845.2:c.66_118del
XM_011542840.3:c.4110_4162del
XM_011542842.3:c.3945_3997del
XM_011542843.2:c.4110_4162del
XM_011542844.3:c.3066_3118del
XM_011542845.2:c.2802_2854del
XM_017017789.2:c.4110_4162del
XM_017017790.2:c.4110_4162del
XM_017017791.1:c.4110_4162del
XM_017017792.2:c.4110_4162del
XR_002957150.1:n.4843_4895del
NM_001351834.2:c.4110_4162del
NM_000051.4:c.4110_4162del