Canonical Allele Identifier: CA1998783294
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108267286A= , CM000673.2:g.108267286A= GRCh38
NC_000011.9:g.108138013A= , CM000673.1:g.108138013A= GRCh37
NC_000011.8:g.107643223A= NCBI36
NG_009830.1:g.49455A= , LRG_135:g.49455A=

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.2582A= ENSP00000388058.2:p.Tyr861=
ENST00000713593.1:c.*2053A= ENSP00000518889.1:n.*2053A=
ENST00000278616.9:c.2582A= ENSP00000278616.4:p.Tyr861=
ENST00000682516.1:n.2716A=
ENST00000683174.1:n.2732A=
ENST00000683605.1:n.2077A=
ENST00000684037.1:c.*1517A= ENSP00000508245.1:n.*1517A=
ENST00000527805.6:c.2582A= ENSP00000435747.2:p.Tyr861=
ENST00000675595.1:c.2417A= ENSP00000502563.1:p.Tyr806=
ENST00000675843.1:c.2582A= MANE Select ENSP00000501606.1:p.Tyr861=
ENST00000278616.8:c.2582A= ENSP00000278616.4:p.Tyr861=
ENST00000452508.6:c.2582A= ENSP00000388058.2:p.Tyr861=
ENST00000527805.5:c.2582A= ENSP00000435747.1:p.Tyr861=
NM_000051.3:c.2582A= , LRG_135t1:c.2582A= NP_000042.3:p.Tyr861=
XM_005271561.3:c.2582A= XP_005271618.2:p.Tyr861=
XM_005271562.3:c.2582A= XP_005271619.2:p.Tyr861=
XM_006718843.2:c.2582A= XP_006718906.1:p.Tyr861=
XM_011542840.1:c.2582A= XP_011541142.1:p.Tyr861=
XM_011542841.1:c.2582A= XP_011541143.1:p.Tyr861=
XM_011542842.1:c.2417A= XP_011541144.1:p.Tyr806=
XM_011542843.1:c.2582A= XP_011541145.1:p.Tyr861=
XM_011542844.1:c.1538A= XP_011541146.1:p.Tyr513=
XM_011542845.1:c.1274A= XP_011541147.1:p.Tyr425=
XM_011542846.1:c.2582A= XP_011541148.1:p.Tyr861=
NM_001351834.1:c.2582A= NP_001338763.1:p.Tyr861=
XM_005271562.5:c.2582A= XP_005271619.2:p.Tyr861=
XM_006718843.4:c.2582A= XP_006718906.1:p.Tyr861=
XM_011542840.3:c.2582A= XP_011541142.1:p.Tyr861=
XM_011542842.3:c.2417A= XP_011541144.1:p.Tyr806=
XM_011542843.2:c.2582A= XP_011541145.1:p.Tyr861=
XM_011542844.3:c.1538A= XP_011541146.1:p.Tyr513=
XM_011542845.2:c.1274A= XP_011541147.1:p.Tyr425=
XM_017017789.2:c.2582A= XP_016873278.1:p.Tyr861=
XM_017017790.2:c.2582A= XP_016873279.1:p.Tyr861=
XM_017017791.1:c.2582A= XP_016873280.1:p.Tyr861=
XM_017017792.2:c.2582A= XP_016873281.1:p.Tyr861=
XR_002957150.1:n.3315A=
NM_001351834.2:c.2582A= NP_001338763.1:p.Tyr861=
NM_000051.4:c.2582A= MANE Select NP_000042.3:p.Tyr861=