Canonical Allele Identifier: CA1139662162

Gene: ATM

Linked Data

• ClinVar Variation Id: 982023
• ClinVar RCV Id: RCV001261516
• dbSNP Id: rs2080292910

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108253829dup , CM000673.2:g.108253829dup	GRCh38
NC_000011.9:g.108124556dup , CM000673.1:g.108124556dup	GRCh37
NC_000011.8:g.107629766dup	NCBI36
NG_009830.1:g.35998dup , LRG_135:g.35998dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.1914dup	ENSP00000388058.2:p.Asp639ArgfsTer2
ENST00000713593.1:c.*1385dup	ENSP00000518889.1:n.*1385dup
ENST00000278616.9:c.1914dup	ENSP00000278616.4:p.Asp639ArgfsTer2
ENST00000682516.1:n.2048dup
ENST00000683174.1:n.2064dup
ENST00000683605.1:n.1409dup
ENST00000684037.1:c.*849dup	ENSP00000508245.1:n.*849dup
ENST00000684061.1:n.2048dup
ENST00000527805.6:c.1914dup	ENSP00000435747.2:p.Asp639ArgfsTer2
ENST00000675595.1:c.1749dup	ENSP00000502563.1:p.Asp584ArgfsTer2
ENST00000675843.1:c.1914dup MANE Select	ENSP00000501606.1:p.Asp639ArgfsTer2
ENST00000278616.8:c.1914dup	ENSP00000278616.4:p.Asp639ArgfsTer2
ENST00000452508.6:c.1914dup	ENSP00000388058.2:p.Asp639ArgfsTer2
ENST00000525012.5:n.93-2dup
ENST00000527805.5:c.1914dup	ENSP00000435747.1:p.Asp639ArgfsTer2
ENST00000533526.1:n.93-26dup
NM_000051.3:c.1914dup , LRG_135t1:c.1914dup	NP_000042.3:p.Asp639ArgfsTer2
XM_005271561.3:c.1914dup	XP_005271618.2:p.Asp639ArgfsTer2
XM_005271562.3:c.1914dup	XP_005271619.2:p.Asp639ArgfsTer2
XM_006718843.2:c.1914dup	XP_006718906.1:p.Asp639ArgfsTer2
XM_011542840.1:c.1914dup	XP_011541142.1:p.Asp639ArgfsTer2
XM_011542841.1:c.1914dup	XP_011541143.1:p.Asp639ArgfsTer2
XM_011542842.1:c.1749dup	XP_011541144.1:p.Asp584ArgfsTer2
XM_011542843.1:c.1914dup	XP_011541145.1:p.Asp639ArgfsTer2
XM_011542844.1:c.870dup	XP_011541146.1:p.Asp291ArgfsTer2
XM_011542845.1:c.606dup	XP_011541147.1:p.Asp203ArgfsTer2
XM_011542846.1:c.1914dup	XP_011541148.1:p.Asp639ArgfsTer2
NM_001351834.1:c.1914dup	NP_001338763.1:p.Asp639ArgfsTer2
XM_005271562.5:c.1914dup	XP_005271619.2:p.Asp639ArgfsTer2
XM_006718843.4:c.1914dup	XP_006718906.1:p.Asp639ArgfsTer2
XM_011542840.3:c.1914dup	XP_011541142.1:p.Asp639ArgfsTer2
XM_011542842.3:c.1749dup	XP_011541144.1:p.Asp584ArgfsTer2
XM_011542843.2:c.1914dup	XP_011541145.1:p.Asp639ArgfsTer2
XM_011542844.3:c.870dup	XP_011541146.1:p.Asp291ArgfsTer2
XM_011542845.2:c.606dup	XP_011541147.1:p.Asp203ArgfsTer2
XM_017017789.2:c.1914dup	XP_016873278.1:p.Asp639ArgfsTer2
XM_017017790.2:c.1914dup	XP_016873279.1:p.Asp639ArgfsTer2
XM_017017791.1:c.1914dup	XP_016873280.1:p.Asp639ArgfsTer2
XM_017017792.2:c.1914dup	XP_016873281.1:p.Asp639ArgfsTer2
XR_002957150.1:n.2647dup
NM_001351834.2:c.1914dup	NP_001338763.1:p.Asp639ArgfsTer2
NM_000051.4:c.1914dup MANE Select	NP_000042.3:p.Asp639ArgfsTer2