Canonical Allele Identifier: CA1998799692
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108302878A= , CM000673.2:g.108302878A= GRCh38
NC_000011.9:g.108173605A= , CM000673.1:g.108173605A= GRCh37
NC_000011.8:g.107678815A= NCBI36
NG_009830.1:g.85047A= , LRG_135:g.85047A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.5345A= ENSP00000388058.2:p.Lys1782=
ENST00000713593.1:c.*4816A= ENSP00000518889.1:n.*4816A=
ENST00000278616.9:c.5345A= ENSP00000278616.4:p.Lys1782=
ENST00000683174.1:n.6829A=
ENST00000683524.1:n.569A=
ENST00000684152.1:n.1059A=
ENST00000527805.6:c.*409A= ENSP00000435747.2:n.*409A=
ENST00000675595.1:c.*409A= ENSP00000502563.1:n.*409A=
ENST00000675843.1:c.5345A= MANE Select ENSP00000501606.1:p.Lys1782=
ENST00000278616.8:c.5345A= ENSP00000278616.4:p.Lys1782=
ENST00000452508.6:c.5345A= ENSP00000388058.2:p.Lys1782=
ENST00000524792.5:n.1560A=
ENST00000533690.5:n.749A=
ENST00000534625.1:n.574A=
NM_000051.3:c.5345A= , LRG_135t1:c.5345A= NP_000042.3:p.Lys1782=
XM_005271561.3:c.5345A= XP_005271618.2:p.Lys1782=
XM_005271562.3:c.5345A= XP_005271619.2:p.Lys1782=
XM_006718843.2:c.5345A= XP_006718906.1:p.Lys1782=
XM_006718845.1:c.1301A= XP_006718908.1:p.Lys434=
XM_011542840.1:c.5345A= XP_011541142.1:p.Lys1782=
XM_011542841.1:c.5345A= XP_011541143.1:p.Lys1782=
XM_011542842.1:c.5180A= XP_011541144.1:p.Lys1727=
XM_011542843.1:c.5345A= XP_011541145.1:p.Lys1782=
XM_011542844.1:c.4301A= XP_011541146.1:p.Lys1434=
XM_011542845.1:c.4037A= XP_011541147.1:p.Lys1346=
XM_011542846.1:c.*3A= XP_011541148.1:n.*3A=
XM_011542847.1:c.416A= XP_011541149.1:p.Lys139=
NM_001351834.1:c.5345A= NP_001338763.1:p.Lys1782=
XM_005271562.5:c.5345A= XP_005271619.2:p.Lys1782=
XM_006718843.4:c.5345A= XP_006718906.1:p.Lys1782=
XM_006718845.2:c.1301A= XP_006718908.1:p.Lys434=
XM_011542840.3:c.5345A= XP_011541142.1:p.Lys1782=
XM_011542842.3:c.5180A= XP_011541144.1:p.Lys1727=
XM_011542843.2:c.5345A= XP_011541145.1:p.Lys1782=
XM_011542844.3:c.4301A= XP_011541146.1:p.Lys1434=
XM_011542845.2:c.4037A= XP_011541147.1:p.Lys1346=
XM_017017789.2:c.5345A= XP_016873278.1:p.Lys1782=
XM_017017790.2:c.5345A= XP_016873279.1:p.Lys1782=
XM_017017791.1:c.5345A= XP_016873280.1:p.Lys1782=
XM_017017792.2:c.*26A= XP_016873281.1:n.*26A=
XR_002957150.1:n.5945A=
NM_001351834.2:c.5345A= NP_001338763.1:p.Lys1782=
NM_000051.4:c.5345A= MANE Select NP_000042.3:p.Lys1782=