Canonical Allele Identifier: CA10579188
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 233138
dbSNP Id: rs587782239

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108304796G>A , CM000673.2:g.108304796G>A GRCh38
NC_000011.9:g.108175523G>A , CM000673.1:g.108175523G>A GRCh37
NC_000011.8:g.107680733G>A NCBI36
NG_009830.1:g.86965G>A , LRG_135:g.86965G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.5618G>A ENSP00000388058.2:p.Cys1873Tyr
ENST00000713593.1:c.*5089G>A ENSP00000518889.1:n.*5089G>A
ENST00000278616.9:c.5618G>A ENSP00000278616.4:p.Cys1873Tyr
ENST00000683174.1:n.7102G>A
ENST00000683524.1:n.842G>A
ENST00000684152.1:n.1332G>A
ENST00000527805.6:c.*682G>A ENSP00000435747.2:n.*682G>A
ENST00000675595.1:c.*682G>A ENSP00000502563.1:n.*682G>A
ENST00000675843.1:c.5618G>A MANE Select ENSP00000501606.1:p.Cys1873Tyr
ENST00000278616.8:c.5618G>A ENSP00000278616.4:p.Cys1873Tyr
ENST00000452508.6:c.5618G>A ENSP00000388058.2:p.Cys1873Tyr
ENST00000524792.5:n.1833G>A
ENST00000529588.5:c.130G>A
ENST00000533690.5:n.1022G>A
NM_000051.3:c.5618G>A , LRG_135t1:c.5618G>A NP_000042.3:p.Cys1873Tyr
XM_005271561.3:c.5618G>A XP_005271618.2:p.Cys1873Tyr
XM_005271562.3:c.5618G>A XP_005271619.2:p.Cys1873Tyr
XM_006718843.2:c.5618G>A XP_006718906.1:p.Cys1873Tyr
XM_006718845.1:c.1574G>A XP_006718908.1:p.Cys525Tyr
XM_011542840.1:c.5618G>A XP_011541142.1:p.Cys1873Tyr
XM_011542841.1:c.5618G>A XP_011541143.1:p.Cys1873Tyr
XM_011542842.1:c.5453G>A XP_011541144.1:p.Cys1818Tyr
XM_011542843.1:c.5618G>A XP_011541145.1:p.Cys1873Tyr
XM_011542844.1:c.4574G>A XP_011541146.1:p.Cys1525Tyr
XM_011542845.1:c.4310G>A XP_011541147.1:p.Cys1437Tyr
XM_011542847.1:c.689G>A XP_011541149.1:p.Cys230Tyr
NM_001351834.1:c.5618G>A NP_001338763.1:p.Cys1873Tyr
XM_005271562.5:c.5618G>A XP_005271619.2:p.Cys1873Tyr
XM_006718843.4:c.5618G>A XP_006718906.1:p.Cys1873Tyr
XM_006718845.2:c.1574G>A XP_006718908.1:p.Cys525Tyr
XM_011542840.3:c.5618G>A XP_011541142.1:p.Cys1873Tyr
XM_011542842.3:c.5453G>A XP_011541144.1:p.Cys1818Tyr
XM_011542843.2:c.5618G>A XP_011541145.1:p.Cys1873Tyr
XM_011542844.3:c.4574G>A XP_011541146.1:p.Cys1525Tyr
XM_011542845.2:c.4310G>A XP_011541147.1:p.Cys1437Tyr
XM_017017789.2:c.5618G>A XP_016873278.1:p.Cys1873Tyr
XM_017017790.2:c.5618G>A XP_016873279.1:p.Cys1873Tyr
XM_017017791.1:c.5618G>A XP_016873280.1:p.Cys1873Tyr
XR_002957150.1:n.6218G>A
NM_001351834.2:c.5618G>A NP_001338763.1:p.Cys1873Tyr
NM_000051.4:c.5618G>A MANE Select NP_000042.3:p.Cys1873Tyr