Canonical Allele Identifier: CA1998799728
Gene: ATM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108302886C= , CM000673.2:g.108302886C= GRCh38
NC_000011.9:g.108173613C= , CM000673.1:g.108173613C= GRCh37
NC_000011.8:g.107678823C= NCBI36
NG_009830.1:g.85055C= , LRG_135:g.85055C=

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.5353C= ENSP00000388058.2:p.Pro1785=
ENST00000713593.1:c.*4824C= ENSP00000518889.1:n.*4824C=
ENST00000278616.9:c.5353C= ENSP00000278616.4:p.Pro1785=
ENST00000683174.1:n.6837C=
ENST00000683524.1:n.577C=
ENST00000684152.1:n.1067C=
ENST00000527805.6:c.*417C= ENSP00000435747.2:n.*417C=
ENST00000675595.1:c.*417C= ENSP00000502563.1:n.*417C=
ENST00000675843.1:c.5353C= MANE Select ENSP00000501606.1:p.Pro1785=
ENST00000278616.8:c.5353C= ENSP00000278616.4:p.Pro1785=
ENST00000452508.6:c.5353C= ENSP00000388058.2:p.Pro1785=
ENST00000524792.5:n.1568C=
ENST00000533690.5:n.757C=
ENST00000534625.1:n.582C=
NM_000051.3:c.5353C= , LRG_135t1:c.5353C= NP_000042.3:p.Pro1785=
XM_005271561.3:c.5353C= XP_005271618.2:p.Pro1785=
XM_005271562.3:c.5353C= XP_005271619.2:p.Pro1785=
XM_006718843.2:c.5353C= XP_006718906.1:p.Pro1785=
XM_006718845.1:c.1309C= XP_006718908.1:p.Pro437=
XM_011542840.1:c.5353C= XP_011541142.1:p.Pro1785=
XM_011542841.1:c.5353C= XP_011541143.1:p.Pro1785=
XM_011542842.1:c.5188C= XP_011541144.1:p.Pro1730=
XM_011542843.1:c.5353C= XP_011541145.1:p.Pro1785=
XM_011542844.1:c.4309C= XP_011541146.1:p.Pro1437=
XM_011542845.1:c.4045C= XP_011541147.1:p.Pro1349=
XM_011542846.1:c.*11C= XP_011541148.1:n.*11C=
XM_011542847.1:c.424C= XP_011541149.1:p.Pro142=
NM_001351834.1:c.5353C= NP_001338763.1:p.Pro1785=
XM_005271562.5:c.5353C= XP_005271619.2:p.Pro1785=
XM_006718843.4:c.5353C= XP_006718906.1:p.Pro1785=
XM_006718845.2:c.1309C= XP_006718908.1:p.Pro437=
XM_011542840.3:c.5353C= XP_011541142.1:p.Pro1785=
XM_011542842.3:c.5188C= XP_011541144.1:p.Pro1730=
XM_011542843.2:c.5353C= XP_011541145.1:p.Pro1785=
XM_011542844.3:c.4309C= XP_011541146.1:p.Pro1437=
XM_011542845.2:c.4045C= XP_011541147.1:p.Pro1349=
XM_017017789.2:c.5353C= XP_016873278.1:p.Pro1785=
XM_017017790.2:c.5353C= XP_016873279.1:p.Pro1785=
XM_017017791.1:c.5353C= XP_016873280.1:p.Pro1785=
XM_017017792.2:c.*34C= XP_016873281.1:n.*34C=
XR_002957150.1:n.5953C=
NM_001351834.2:c.5353C= NP_001338763.1:p.Pro1785=
NM_000051.4:c.5353C= MANE Select NP_000042.3:p.Pro1785=