Canonical Allele Identifier: CA1998801197
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108304681A= , CM000673.2:g.108304681A= GRCh38
NC_000011.9:g.108175408A= , CM000673.1:g.108175408A= GRCh37
NC_000011.8:g.107680618A= NCBI36
NG_009830.1:g.86850A= , LRG_135:g.86850A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.5503A= ENSP00000388058.2:p.Thr1835=
ENST00000713593.1:c.*4974A= ENSP00000518889.1:n.*4974A=
ENST00000278616.9:c.5503A= ENSP00000278616.4:p.Thr1835=
ENST00000683174.1:n.6987A=
ENST00000683524.1:n.727A=
ENST00000684152.1:n.1217A=
ENST00000527805.6:c.*567A= ENSP00000435747.2:n.*567A=
ENST00000675595.1:c.*567A= ENSP00000502563.1:n.*567A=
ENST00000675843.1:c.5503A= MANE Select ENSP00000501606.1:p.Thr1835=
ENST00000278616.8:c.5503A= ENSP00000278616.4:p.Thr1835=
ENST00000452508.6:c.5503A= ENSP00000388058.2:p.Thr1835=
ENST00000524792.5:n.1718A=
ENST00000529588.5:c.15A=
ENST00000533690.5:n.907A=
NM_000051.3:c.5503A= , LRG_135t1:c.5503A= NP_000042.3:p.Thr1835=
XM_005271561.3:c.5503A= XP_005271618.2:p.Thr1835=
XM_005271562.3:c.5503A= XP_005271619.2:p.Thr1835=
XM_006718843.2:c.5503A= XP_006718906.1:p.Thr1835=
XM_006718845.1:c.1459A= XP_006718908.1:p.Thr487=
XM_011542840.1:c.5503A= XP_011541142.1:p.Thr1835=
XM_011542841.1:c.5503A= XP_011541143.1:p.Thr1835=
XM_011542842.1:c.5338A= XP_011541144.1:p.Thr1780=
XM_011542843.1:c.5503A= XP_011541145.1:p.Thr1835=
XM_011542844.1:c.4459A= XP_011541146.1:p.Thr1487=
XM_011542845.1:c.4195A= XP_011541147.1:p.Thr1399=
XM_011542847.1:c.574A= XP_011541149.1:p.Thr192=
NM_001351834.1:c.5503A= NP_001338763.1:p.Thr1835=
XM_005271562.5:c.5503A= XP_005271619.2:p.Thr1835=
XM_006718843.4:c.5503A= XP_006718906.1:p.Thr1835=
XM_006718845.2:c.1459A= XP_006718908.1:p.Thr487=
XM_011542840.3:c.5503A= XP_011541142.1:p.Thr1835=
XM_011542842.3:c.5338A= XP_011541144.1:p.Thr1780=
XM_011542843.2:c.5503A= XP_011541145.1:p.Thr1835=
XM_011542844.3:c.4459A= XP_011541146.1:p.Thr1487=
XM_011542845.2:c.4195A= XP_011541147.1:p.Thr1399=
XM_017017789.2:c.5503A= XP_016873278.1:p.Thr1835=
XM_017017790.2:c.5503A= XP_016873279.1:p.Thr1835=
XM_017017791.1:c.5503A= XP_016873280.1:p.Thr1835=
XR_002957150.1:n.6103A=
NM_001351834.2:c.5503A= NP_001338763.1:p.Thr1835=
NM_000051.4:c.5503A= MANE Select NP_000042.3:p.Thr1835=