Canonical Allele Identifier: CA2580083207
Community Standard Title: NC_000011.10:g.108271135_108271156del
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108271135_108271156del , CM000673.2:g.108271135_108271156del GRCh38
NC_000011.9:g.108141862_108141883del , CM000673.1:g.108141862_108141883del GRCh37
NC_000011.8:g.107647072_107647093del NCBI36
NG_009830.1:g.53304_53325del , LRG_135:g.53304_53325del

Transcript Alleles

HGVS Amino-acid Change
NM_000051.3:c.2910_2921+10del , LRG_135t1:c.2910_2921+10del
NM_000051.4:c.2910_2921+10del
NM_001351834.1:c.2910_2921+10del
NM_001351834.2:c.2910_2921+10del
ENST00000278616.8:c.2910_2921+10del
ENST00000278616.9:c.2910_2921+10del
ENST00000419286.2:n.201-116_201-95del
ENST00000452508.6:c.2910_2921+10del
ENST00000452508.7:c.2910_2921+10del
ENST00000527805.5:c.2910_2921+10del
ENST00000527805.6:c.2910_2921+10del
ENST00000675595.1:c.2745_2756+10del
ENST00000675843.1:c.2910_2921+10del
ENST00000682516.1:n.2844_2855+10del
ENST00000683174.1:n.3060_3071+10del
ENST00000684037.1:c.*1645_*1656+10del
ENST00000713593.1:c.*2381_*2392+10del
XM_005271561.3:c.2910_2921+10del
XM_005271562.3:c.2910_2921+10del
XM_005271562.5:c.2910_2921+10del
XM_006718843.2:c.2910_2921+10del
XM_006718843.4:c.2910_2921+10del
XM_011542840.1:c.2910_2921+10del
XM_011542840.3:c.2910_2921+10del
XM_011542841.1:c.2910_2921+10del
XM_011542842.1:c.2745_2756+10del
XM_011542842.3:c.2745_2756+10del
XM_011542843.1:c.2910_2921+10del
XM_011542843.2:c.2910_2921+10del
XM_011542844.1:c.1866_1877+10del
XM_011542844.3:c.1866_1877+10del
XM_011542845.1:c.1602_1613+10del
XM_011542845.2:c.1602_1613+10del
XM_011542846.1:c.2910_2921+10del
XM_017017789.2:c.2910_2921+10del
XM_017017790.2:c.2910_2921+10del
XM_017017791.1:c.2910_2921+10del
XM_017017792.2:c.2910_2921+10del
XR_002957150.1:n.3643_3654+10del