Canonical Allele Identifier: CA382537011

Gene: ATM

Linked Data

• ClinVar Variation Id: 1784106
• ClinVar RCV Id: RCV002417043
• MyVariant Identifiers: chr11:g.108124641A>G (hg19) ; chr11:g.108253914A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108253914A>G , CM000673.2:g.108253914A>G	GRCh38
NC_000011.9:g.108124641A>G , CM000673.1:g.108124641A>G	GRCh37
NC_000011.8:g.107629851A>G	NCBI36
NG_009830.1:g.36083A>G , LRG_135:g.36083A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.1999A>G	ENSP00000388058.2:p.Arg667Gly
ENST00000713593.1:c.*1470A>G	ENSP00000518889.1:n.*1470A>G
ENST00000278616.9:c.1999A>G	ENSP00000278616.4:p.Arg667Gly
ENST00000682516.1:n.2133A>G
ENST00000683174.1:n.2149A>G
ENST00000683605.1:n.1494A>G
ENST00000684037.1:c.*934A>G	ENSP00000508245.1:n.*934A>G
ENST00000684061.1:n.2133A>G
ENST00000527805.6:c.1999A>G	ENSP00000435747.2:p.Arg667Gly
ENST00000675595.1:c.1834A>G	ENSP00000502563.1:p.Arg612Gly
ENST00000675843.1:c.1999A>G MANE Select	ENSP00000501606.1:p.Arg667Gly
ENST00000278616.8:c.1999A>G	ENSP00000278616.4:p.Arg667Gly
ENST00000452508.6:c.1999A>G	ENSP00000388058.2:p.Arg667Gly
ENST00000525012.5:n.176A>G
ENST00000527805.5:c.1999A>G	ENSP00000435747.1:p.Arg667Gly
ENST00000533526.1:n.152A>G
NM_000051.3:c.1999A>G , LRG_135t1:c.1999A>G	NP_000042.3:p.Arg667Gly
XM_005271561.3:c.1999A>G	XP_005271618.2:p.Arg667Gly
XM_005271562.3:c.1999A>G	XP_005271619.2:p.Arg667Gly
XM_006718843.2:c.1999A>G	XP_006718906.1:p.Arg667Gly
XM_011542840.1:c.1999A>G	XP_011541142.1:p.Arg667Gly
XM_011542841.1:c.1999A>G	XP_011541143.1:p.Arg667Gly
XM_011542842.1:c.1834A>G	XP_011541144.1:p.Arg612Gly
XM_011542843.1:c.1999A>G	XP_011541145.1:p.Arg667Gly
XM_011542844.1:c.955A>G	XP_011541146.1:p.Arg319Gly
XM_011542845.1:c.691A>G	XP_011541147.1:p.Arg231Gly
XM_011542846.1:c.1999A>G	XP_011541148.1:p.Arg667Gly
NM_001351834.1:c.1999A>G	NP_001338763.1:p.Arg667Gly
XM_005271562.5:c.1999A>G	XP_005271619.2:p.Arg667Gly
XM_006718843.4:c.1999A>G	XP_006718906.1:p.Arg667Gly
XM_011542840.3:c.1999A>G	XP_011541142.1:p.Arg667Gly
XM_011542842.3:c.1834A>G	XP_011541144.1:p.Arg612Gly
XM_011542843.2:c.1999A>G	XP_011541145.1:p.Arg667Gly
XM_011542844.3:c.955A>G	XP_011541146.1:p.Arg319Gly
XM_011542845.2:c.691A>G	XP_011541147.1:p.Arg231Gly
XM_017017789.2:c.1999A>G	XP_016873278.1:p.Arg667Gly
XM_017017790.2:c.1999A>G	XP_016873279.1:p.Arg667Gly
XM_017017791.1:c.1999A>G	XP_016873280.1:p.Arg667Gly
XM_017017792.2:c.1999A>G	XP_016873281.1:p.Arg667Gly
XR_002957150.1:n.2732A>G
NM_001351834.2:c.1999A>G	NP_001338763.1:p.Arg667Gly
NM_000051.4:c.1999A>G MANE Select	NP_000042.3:p.Arg667Gly