Canonical Allele Identifier: CA382524176
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481233
ClinVar RCV Id: RCV000563090
dbSNP Id: rs1555093268

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108284228T>A , CM000673.2:g.108284228T>A GRCh38
NC_000011.9:g.108154955T>A , CM000673.1:g.108154955T>A GRCh37
NC_000011.8:g.107660165T>A NCBI36
NG_009830.1:g.66397T>A , LRG_135:g.66397T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.3748T>A ENSP00000388058.2:p.Ser1250Thr
ENST00000713593.1:c.*3219T>A ENSP00000518889.1:n.*3219T>A
ENST00000278616.9:c.3748T>A ENSP00000278616.4:p.Ser1250Thr
ENST00000682289.1:n.95T>A
ENST00000683174.1:n.3898T>A
ENST00000527805.6:c.3748T>A ENSP00000435747.2:p.Ser1250Thr
ENST00000675595.1:c.3583T>A ENSP00000502563.1:p.Ser1195Thr
ENST00000675843.1:c.3748T>A MANE Select ENSP00000501606.1:p.Ser1250Thr
ENST00000278616.8:c.3748T>A ENSP00000278616.4:p.Ser1250Thr
ENST00000452508.6:c.3748T>A ENSP00000388058.2:p.Ser1250Thr
ENST00000527805.5:c.3748T>A ENSP00000435747.1:p.Ser1250Thr
NM_000051.3:c.3748T>A , LRG_135t1:c.3748T>A NP_000042.3:p.Ser1250Thr
XM_005271561.3:c.3748T>A XP_005271618.2:p.Ser1250Thr
XM_005271562.3:c.3748T>A XP_005271619.2:p.Ser1250Thr
XM_006718843.2:c.3748T>A XP_006718906.1:p.Ser1250Thr
XM_011542840.1:c.3748T>A XP_011541142.1:p.Ser1250Thr
XM_011542841.1:c.3748T>A XP_011541143.1:p.Ser1250Thr
XM_011542842.1:c.3583T>A XP_011541144.1:p.Ser1195Thr
XM_011542843.1:c.3748T>A XP_011541145.1:p.Ser1250Thr
XM_011542844.1:c.2704T>A XP_011541146.1:p.Ser902Thr
XM_011542845.1:c.2440T>A XP_011541147.1:p.Ser814Thr
XM_011542846.1:c.3748T>A XP_011541148.1:p.Ser1250Thr
NM_001351834.1:c.3748T>A NP_001338763.1:p.Ser1250Thr
XM_005271562.5:c.3748T>A XP_005271619.2:p.Ser1250Thr
XM_006718843.4:c.3748T>A XP_006718906.1:p.Ser1250Thr
XM_011542840.3:c.3748T>A XP_011541142.1:p.Ser1250Thr
XM_011542842.3:c.3583T>A XP_011541144.1:p.Ser1195Thr
XM_011542843.2:c.3748T>A XP_011541145.1:p.Ser1250Thr
XM_011542844.3:c.2704T>A XP_011541146.1:p.Ser902Thr
XM_011542845.2:c.2440T>A XP_011541147.1:p.Ser814Thr
XM_017017789.2:c.3748T>A XP_016873278.1:p.Ser1250Thr
XM_017017790.2:c.3748T>A XP_016873279.1:p.Ser1250Thr
XM_017017791.1:c.3748T>A XP_016873280.1:p.Ser1250Thr
XM_017017792.2:c.3748T>A XP_016873281.1:p.Ser1250Thr
XR_002957150.1:n.4481T>A
NM_001351834.2:c.3748T>A NP_001338763.1:p.Ser1250Thr
NM_000051.4:c.3748T>A MANE Select NP_000042.3:p.Ser1250Thr