Canonical Allele Identifier: CA382530773
Gene: ATM HGNC NCBI

Linked Data

dbSNP Id: rs2079880133

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108247002A>T , CM000673.2:g.108247002A>T GRCh38
NC_000011.9:g.108117729A>T , CM000673.1:g.108117729A>T GRCh37
NC_000011.8:g.107622939A>T NCBI36
NG_009830.1:g.29171A>T , LRG_135:g.29171A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.940A>T ENSP00000388058.2:p.Asn314Tyr
ENST00000713593.1:c.*411A>T ENSP00000518889.1:n.*411A>T
ENST00000278616.9:c.940A>T ENSP00000278616.4:p.Asn314Tyr
ENST00000682516.1:n.1074A>T
ENST00000682956.1:n.1074A>T
ENST00000683100.1:n.3287A>T
ENST00000683174.1:n.1090A>T
ENST00000683605.1:n.435A>T
ENST00000684037.1:c.940A>T ENSP00000508245.1:p.Asn314Tyr
ENST00000684061.1:n.1074A>T
ENST00000684179.1:n.909A>T
ENST00000527805.6:c.940A>T ENSP00000435747.2:p.Asn314Tyr
ENST00000675595.1:c.775A>T ENSP00000502563.1:p.Asn259Tyr
ENST00000675843.1:c.940A>T MANE Select ENSP00000501606.1:p.Asn314Tyr
ENST00000278616.8:c.940A>T ENSP00000278616.4:p.Asn314Tyr
ENST00000452508.6:c.940A>T ENSP00000388058.2:p.Asn314Tyr
ENST00000527805.5:c.940A>T ENSP00000435747.1:p.Asn314Tyr
NM_000051.3:c.940A>T , LRG_135t1:c.940A>T NP_000042.3:p.Asn314Tyr
XM_005271561.3:c.940A>T XP_005271618.2:p.Asn314Tyr
XM_005271562.3:c.940A>T XP_005271619.2:p.Asn314Tyr
XM_006718843.2:c.940A>T XP_006718906.1:p.Asn314Tyr
XM_011542840.1:c.940A>T XP_011541142.1:p.Asn314Tyr
XM_011542841.1:c.940A>T XP_011541143.1:p.Asn314Tyr
XM_011542842.1:c.775A>T XP_011541144.1:p.Asn259Tyr
XM_011542843.1:c.940A>T XP_011541145.1:p.Asn314Tyr
XM_011542844.1:c.-105A>T XP_011541146.1:n.-105A>T
XM_011542846.1:c.940A>T XP_011541148.1:p.Asn314Tyr
NM_001351834.1:c.940A>T NP_001338763.1:p.Asn314Tyr
XM_005271562.5:c.940A>T XP_005271619.2:p.Asn314Tyr
XM_006718843.4:c.940A>T XP_006718906.1:p.Asn314Tyr
XM_011542840.3:c.940A>T XP_011541142.1:p.Asn314Tyr
XM_011542842.3:c.775A>T XP_011541144.1:p.Asn259Tyr
XM_011542843.2:c.940A>T XP_011541145.1:p.Asn314Tyr
XM_011542844.3:c.-105A>T XP_011541146.1:n.-105A>T
XM_017017789.2:c.940A>T XP_016873278.1:p.Asn314Tyr
XM_017017790.2:c.940A>T XP_016873279.1:p.Asn314Tyr
XM_017017791.1:c.940A>T XP_016873280.1:p.Asn314Tyr
XM_017017792.2:c.940A>T XP_016873281.1:p.Asn314Tyr
XR_002957150.1:n.1673A>T
NM_001351834.2:c.940A>T NP_001338763.1:p.Asn314Tyr
NM_000051.4:c.940A>T MANE Select NP_000042.3:p.Asn314Tyr