Canonical Allele Identifier: CA228386099

Gene: ATM

Linked Data

• ClinVar Variation Id: 489553
• ClinVar RCV Id: RCV000580017 ; RCV000817816 ; RCV003441964
• dbSNP Id: rs980731959
• MyVariant Identifiers: chr11:g.108170480A>G (hg19) ; chr11:g.108299753A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108299753A>G , CM000673.2:g.108299753A>G	GRCh38
NC_000011.9:g.108170480A>G , CM000673.1:g.108170480A>G	GRCh37
NC_000011.8:g.107675690A>G	NCBI36
NG_009830.1:g.81922A>G , LRG_135:g.81922A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5045A>G	ENSP00000388058.2:p.Asp1682Gly
ENST00000713593.1:c.*4516A>G	ENSP00000518889.1:n.*4516A>G
ENST00000278616.9:c.5045A>G	ENSP00000278616.4:p.Asp1682Gly
ENST00000683174.1:n.6529A>G
ENST00000683524.1:n.269A>G
ENST00000684152.1:n.759A>G
ENST00000527805.6:c.*109A>G	ENSP00000435747.2:n.*109A>G
ENST00000675595.1:c.*109A>G	ENSP00000502563.1:n.*109A>G
ENST00000675843.1:c.5045A>G MANE Select	ENSP00000501606.1:p.Asp1682Gly
ENST00000278616.8:c.5045A>G	ENSP00000278616.4:p.Asp1682Gly
ENST00000452508.6:c.5045A>G	ENSP00000388058.2:p.Asp1682Gly
ENST00000524792.5:n.1260A>G
ENST00000533690.5:n.449A>G
ENST00000534625.1:n.274A>G
NM_000051.3:c.5045A>G , LRG_135t1:c.5045A>G	NP_000042.3:p.Asp1682Gly
XM_005271561.3:c.5045A>G	XP_005271618.2:p.Asp1682Gly
XM_005271562.3:c.5045A>G	XP_005271619.2:p.Asp1682Gly
XM_006718843.2:c.5045A>G	XP_006718906.1:p.Asp1682Gly
XM_006718845.1:c.1001A>G	XP_006718908.1:p.Asp334Gly
XM_011542840.1:c.5045A>G	XP_011541142.1:p.Asp1682Gly
XM_011542841.1:c.5045A>G	XP_011541143.1:p.Asp1682Gly
XM_011542842.1:c.4880A>G	XP_011541144.1:p.Asp1627Gly
XM_011542843.1:c.5045A>G	XP_011541145.1:p.Asp1682Gly
XM_011542844.1:c.4001A>G	XP_011541146.1:p.Asp1334Gly
XM_011542845.1:c.3737A>G	XP_011541147.1:p.Asp1246Gly
XM_011542846.1:c.5045A>G	XP_011541148.1:p.Asp1682Gly
XM_011542847.1:c.116A>G	XP_011541149.1:p.Asp39Gly
NM_001351834.1:c.5045A>G	NP_001338763.1:p.Asp1682Gly
XM_005271562.5:c.5045A>G	XP_005271619.2:p.Asp1682Gly
XM_006718843.4:c.5045A>G	XP_006718906.1:p.Asp1682Gly
XM_006718845.2:c.1001A>G	XP_006718908.1:p.Asp334Gly
XM_011542840.3:c.5045A>G	XP_011541142.1:p.Asp1682Gly
XM_011542842.3:c.4880A>G	XP_011541144.1:p.Asp1627Gly
XM_011542843.2:c.5045A>G	XP_011541145.1:p.Asp1682Gly
XM_011542844.3:c.4001A>G	XP_011541146.1:p.Asp1334Gly
XM_011542845.2:c.3737A>G	XP_011541147.1:p.Asp1246Gly
XM_017017789.2:c.5045A>G	XP_016873278.1:p.Asp1682Gly
XM_017017790.2:c.5045A>G	XP_016873279.1:p.Asp1682Gly
XM_017017791.1:c.5045A>G	XP_016873280.1:p.Asp1682Gly
XM_017017792.2:c.5045A>G	XP_016873281.1:p.Asp1682Gly
XR_002957150.1:n.5645A>G
NM_001351834.2:c.5045A>G	NP_001338763.1:p.Asp1682Gly
NM_000051.4:c.5045A>G MANE Select	NP_000042.3:p.Asp1682Gly