Canonical Allele Identifier: CA191185

Gene: ATM

Linked Data

• ClinVar Variation Id: 185158
• ClinVar RCV Id: RCV000164527 ; RCV000627916 ; RCV000589044 ; RCV002247566
• dbSNP Id: rs786201969
• gnomAD v4: 11-108250948-A-G
• MyVariant Identifiers: chr11:g.108121675A>G (hg19) ; chr11:g.108250948A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108250948A>G , CM000673.2:g.108250948A>G	GRCh38
NC_000011.9:g.108121675A>G , CM000673.1:g.108121675A>G	GRCh37
NC_000011.8:g.107626885A>G	NCBI36
NG_009830.1:g.33117A>G , LRG_135:g.33117A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.1483A>G	ENSP00000388058.2:p.Ile495Val
ENST00000713593.1:c.*954A>G	ENSP00000518889.1:n.*954A>G
ENST00000278616.9:c.1483A>G	ENSP00000278616.4:p.Ile495Val
ENST00000682516.1:n.1617A>G
ENST00000682956.1:n.1617A>G
ENST00000683174.1:n.1633A>G
ENST00000683605.1:n.978A>G
ENST00000684037.1:c.*418A>G	ENSP00000508245.1:n.*418A>G
ENST00000684061.1:n.1617A>G
ENST00000684179.1:n.1452A>G
ENST00000527805.6:c.1483A>G	ENSP00000435747.2:p.Ile495Val
ENST00000675595.1:c.1318A>G	ENSP00000502563.1:p.Ile440Val
ENST00000675843.1:c.1483A>G MANE Select	ENSP00000501606.1:p.Ile495Val
ENST00000278616.8:c.1483A>G	ENSP00000278616.4:p.Ile495Val
ENST00000452508.6:c.1483A>G	ENSP00000388058.2:p.Ile495Val
ENST00000527805.5:c.1483A>G	ENSP00000435747.1:p.Ile495Val
NM_000051.3:c.1483A>G , LRG_135t1:c.1483A>G	NP_000042.3:p.Ile495Val
XM_005271561.3:c.1483A>G	XP_005271618.2:p.Ile495Val
XM_005271562.3:c.1483A>G	XP_005271619.2:p.Ile495Val
XM_006718843.2:c.1483A>G	XP_006718906.1:p.Ile495Val
XM_011542840.1:c.1483A>G	XP_011541142.1:p.Ile495Val
XM_011542841.1:c.1483A>G	XP_011541143.1:p.Ile495Val
XM_011542842.1:c.1318A>G	XP_011541144.1:p.Ile440Val
XM_011542843.1:c.1483A>G	XP_011541145.1:p.Ile495Val
XM_011542844.1:c.439A>G	XP_011541146.1:p.Ile147Val
XM_011542845.1:c.175A>G	XP_011541147.1:p.Ile59Val
XM_011542846.1:c.1483A>G	XP_011541148.1:p.Ile495Val
NM_001351834.1:c.1483A>G	NP_001338763.1:p.Ile495Val
XM_005271562.5:c.1483A>G	XP_005271619.2:p.Ile495Val
XM_006718843.4:c.1483A>G	XP_006718906.1:p.Ile495Val
XM_011542840.3:c.1483A>G	XP_011541142.1:p.Ile495Val
XM_011542842.3:c.1318A>G	XP_011541144.1:p.Ile440Val
XM_011542843.2:c.1483A>G	XP_011541145.1:p.Ile495Val
XM_011542844.3:c.439A>G	XP_011541146.1:p.Ile147Val
XM_011542845.2:c.175A>G	XP_011541147.1:p.Ile59Val
XM_017017789.2:c.1483A>G	XP_016873278.1:p.Ile495Val
XM_017017790.2:c.1483A>G	XP_016873279.1:p.Ile495Val
XM_017017791.1:c.1483A>G	XP_016873280.1:p.Ile495Val
XM_017017792.2:c.1483A>G	XP_016873281.1:p.Ile495Val
XR_002957150.1:n.2216A>G
NM_001351834.2:c.1483A>G	NP_001338763.1:p.Ile495Val
NM_000051.4:c.1483A>G MANE Select	NP_000042.3:p.Ile495Val