Canonical Allele Identifier: CA10603087

Gene: ATM

Linked Data

• ClinVar Variation Id: 280786
• ClinVar RCV Id: RCV000387350 ; RCV000669607 ; RCV002374450
• dbSNP Id: rs886041931
• gnomAD v4: 11-108244786-A-G
• MyVariant Identifiers: chr11:g.108115513A>G (hg19) ; chr11:g.108244786A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108244786A>G , CM000673.2:g.108244786A>G	GRCh38
NC_000011.9:g.108115513A>G , CM000673.1:g.108115513A>G	GRCh37
NC_000011.8:g.107620723A>G	NCBI36
NG_009830.1:g.26955A>G , LRG_135:g.26955A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.663-2A>G	ENSP00000388058.2:n.663-2A>G
ENST00000713593.1:c.*134-2A>G	ENSP00000518889.1:n.*134-2A>G
ENST00000278616.9:c.663-2A>G	ENSP00000278616.4:n.663-2A>G
ENST00000682430.1:n.762-2A>G
ENST00000682516.1:n.797-2A>G
ENST00000682956.1:n.797-2A>G
ENST00000683100.1:n.3008A>G
ENST00000683174.1:n.813-2A>G
ENST00000683605.1:n.158-2A>G
ENST00000684037.1:c.663-2A>G	ENSP00000508245.1:n.663-2A>G
ENST00000684061.1:n.797-2A>G
ENST00000684179.1:n.632-2A>G
ENST00000527805.6:c.663-2A>G	ENSP00000435747.2:n.663-2A>G
ENST00000675595.1:c.498-2A>G	ENSP00000502563.1:n.498-2A>G
ENST00000675843.1:c.663-2A>G MANE Select	ENSP00000501606.1:n.663-2A>G
ENST00000278616.8:c.663-2A>G	ENSP00000278616.4:n.663-2A>G
ENST00000452508.6:c.663-2A>G	ENSP00000388058.2:n.663-2A>G
ENST00000527805.5:c.663-2A>G	ENSP00000435747.1:n.663-2A>G
NM_000051.3:c.663-2A>G , LRG_135t1:c.663-2A>G	NP_000042.3:n.663-2A>G
XM_005271561.3:c.663-2A>G	XP_005271618.2:n.663-2A>G
XM_005271562.3:c.663-2A>G	XP_005271619.2:n.663-2A>G
XM_006718843.2:c.663-2A>G	XP_006718906.1:n.663-2A>G
XM_011542840.1:c.663-2A>G	XP_011541142.1:n.663-2A>G
XM_011542841.1:c.663-2A>G	XP_011541143.1:n.663-2A>G
XM_011542842.1:c.498-2A>G	XP_011541144.1:n.498-2A>G
XM_011542843.1:c.663-2A>G	XP_011541145.1:n.663-2A>G
XM_011542844.1:c.-382-2A>G	XP_011541146.1:n.-382-2A>G
XM_011542846.1:c.663-2A>G	XP_011541148.1:n.663-2A>G
NM_001351834.1:c.663-2A>G	NP_001338763.1:n.663-2A>G
XM_005271562.5:c.663-2A>G	XP_005271619.2:n.663-2A>G
XM_006718843.4:c.663-2A>G	XP_006718906.1:n.663-2A>G
XM_011542840.3:c.663-2A>G	XP_011541142.1:n.663-2A>G
XM_011542842.3:c.498-2A>G	XP_011541144.1:n.498-2A>G
XM_011542843.2:c.663-2A>G	XP_011541145.1:n.663-2A>G
XM_011542844.3:c.-382-2A>G	XP_011541146.1:n.-382-2A>G
XM_017017789.2:c.663-2A>G	XP_016873278.1:n.663-2A>G
XM_017017790.2:c.663-2A>G	XP_016873279.1:n.663-2A>G
XM_017017791.1:c.663-2A>G	XP_016873280.1:n.663-2A>G
XM_017017792.2:c.663-2A>G	XP_016873281.1:n.663-2A>G
XR_002957150.1:n.1396-2A>G
NM_001351834.2:c.663-2A>G	NP_001338763.1:n.663-2A>G
NM_000051.4:c.663-2A>G MANE Select	NP_000042.3:n.663-2A>G