Canonical Allele Identifier: CA1998793480
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108297298G= , CM000673.2:g.108297298G= GRCh38
NC_000011.9:g.108168025G= , CM000673.1:g.108168025G= GRCh37
NC_000011.8:g.107673235G= NCBI36
NG_009830.1:g.79467G= , LRG_135:g.79467G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.4921G= ENSP00000388058.2:p.Asp1641=
ENST00000713593.1:c.*4392G= ENSP00000518889.1:n.*4392G=
ENST00000278616.9:c.4921G= ENSP00000278616.4:p.Asp1641=
ENST00000683174.1:n.6405G=
ENST00000683524.1:n.145G=
ENST00000684152.1:n.635G=
ENST00000527805.6:c.4623G= ENSP00000435747.2:p.Lys1541=
ENST00000675595.1:c.4623G= ENSP00000502563.1:p.Lys1541=
ENST00000675843.1:c.4921G= MANE Select ENSP00000501606.1:p.Asp1641=
ENST00000278616.8:c.4921G= ENSP00000278616.4:p.Asp1641=
ENST00000452508.6:c.4921G= ENSP00000388058.2:p.Asp1641=
ENST00000524792.5:n.1136G=
ENST00000533690.5:n.325G=
NM_000051.3:c.4921G= , LRG_135t1:c.4921G= NP_000042.3:p.Asp1641=
XM_005271561.3:c.4921G= XP_005271618.2:p.Asp1641=
XM_005271562.3:c.4921G= XP_005271619.2:p.Asp1641=
XM_006718843.2:c.4921G= XP_006718906.1:p.Asp1641=
XM_006718845.1:c.877G= XP_006718908.1:p.Asp293=
XM_011542840.1:c.4921G= XP_011541142.1:p.Asp1641=
XM_011542841.1:c.4921G= XP_011541143.1:p.Asp1641=
XM_011542842.1:c.4756G= XP_011541144.1:p.Asp1586=
XM_011542843.1:c.4921G= XP_011541145.1:p.Asp1641=
XM_011542844.1:c.3877G= XP_011541146.1:p.Asp1293=
XM_011542845.1:c.3613G= XP_011541147.1:p.Asp1205=
XM_011542846.1:c.4921G= XP_011541148.1:p.Asp1641=
XM_011542847.1:c.-9G= XP_011541149.1:n.-9G=
NM_001351834.1:c.4921G= NP_001338763.1:p.Asp1641=
XM_005271562.5:c.4921G= XP_005271619.2:p.Asp1641=
XM_006718843.4:c.4921G= XP_006718906.1:p.Asp1641=
XM_006718845.2:c.877G= XP_006718908.1:p.Asp293=
XM_011542840.3:c.4921G= XP_011541142.1:p.Asp1641=
XM_011542842.3:c.4756G= XP_011541144.1:p.Asp1586=
XM_011542843.2:c.4921G= XP_011541145.1:p.Asp1641=
XM_011542844.3:c.3877G= XP_011541146.1:p.Asp1293=
XM_011542845.2:c.3613G= XP_011541147.1:p.Asp1205=
XM_017017789.2:c.4921G= XP_016873278.1:p.Asp1641=
XM_017017790.2:c.4921G= XP_016873279.1:p.Asp1641=
XM_017017791.1:c.4921G= XP_016873280.1:p.Asp1641=
XM_017017792.2:c.4921G= XP_016873281.1:p.Asp1641=
XR_002957150.1:n.5521G=
NM_001351834.2:c.4921G= NP_001338763.1:p.Asp1641=
NM_000051.4:c.4921G= MANE Select NP_000042.3:p.Asp1641=