Canonical Allele Identifier: CA382529894

Gene: ATM

Linked Data

• ClinVar Variation Id: 1738125
• ClinVar RCV Id: RCV002333104
• dbSNP Id: rs3092856
• MyVariant Identifiers: chr11:g.108159732C>G (hg19) ; chr11:g.108289005C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108289005C>G , CM000673.2:g.108289005C>G	GRCh38
NC_000011.9:g.108159732C>G , CM000673.1:g.108159732C>G	GRCh37
NC_000011.8:g.107664942C>G	NCBI36
NG_009830.1:g.71174C>G , LRG_135:g.71174C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.4138C>G	ENSP00000388058.2:p.His1380Asp
ENST00000713593.1:c.*3609C>G	ENSP00000518889.1:n.*3609C>G
ENST00000278616.9:c.4138C>G	ENSP00000278616.4:p.His1380Asp
ENST00000533733.6:n.1401C>G
ENST00000683174.1:n.4288C>G
ENST00000527805.6:c.4138C>G	ENSP00000435747.2:p.His1380Asp
ENST00000675595.1:c.3973C>G	ENSP00000502563.1:p.His1325Asp
ENST00000675843.1:c.4138C>G MANE Select	ENSP00000501606.1:p.His1380Asp
ENST00000278616.8:c.4138C>G	ENSP00000278616.4:p.His1380Asp
ENST00000452508.6:c.4138C>G	ENSP00000388058.2:p.His1380Asp
ENST00000524792.5:n.353C>G
ENST00000531525.2:c.145C>G	ENSP00000434327.2:p.His49Asp
ENST00000533733.5:n.567C>G
NM_000051.3:c.4138C>G , LRG_135t1:c.4138C>G	NP_000042.3:p.His1380Asp
XM_005271561.3:c.4138C>G	XP_005271618.2:p.His1380Asp
XM_005271562.3:c.4138C>G	XP_005271619.2:p.His1380Asp
XM_006718843.2:c.4138C>G	XP_006718906.1:p.His1380Asp
XM_006718845.1:c.94C>G	XP_006718908.1:p.His32Asp
XM_011542840.1:c.4138C>G	XP_011541142.1:p.His1380Asp
XM_011542841.1:c.4138C>G	XP_011541143.1:p.His1380Asp
XM_011542842.1:c.3973C>G	XP_011541144.1:p.His1325Asp
XM_011542843.1:c.4138C>G	XP_011541145.1:p.His1380Asp
XM_011542844.1:c.3094C>G	XP_011541146.1:p.His1032Asp
XM_011542845.1:c.2830C>G	XP_011541147.1:p.His944Asp
XM_011542846.1:c.4138C>G	XP_011541148.1:p.His1380Asp
NM_001351834.1:c.4138C>G	NP_001338763.1:p.His1380Asp
XM_005271562.5:c.4138C>G	XP_005271619.2:p.His1380Asp
XM_006718843.4:c.4138C>G	XP_006718906.1:p.His1380Asp
XM_006718845.2:c.94C>G	XP_006718908.1:p.His32Asp
XM_011542840.3:c.4138C>G	XP_011541142.1:p.His1380Asp
XM_011542842.3:c.3973C>G	XP_011541144.1:p.His1325Asp
XM_011542843.2:c.4138C>G	XP_011541145.1:p.His1380Asp
XM_011542844.3:c.3094C>G	XP_011541146.1:p.His1032Asp
XM_011542845.2:c.2830C>G	XP_011541147.1:p.His944Asp
XM_017017789.2:c.4138C>G	XP_016873278.1:p.His1380Asp
XM_017017790.2:c.4138C>G	XP_016873279.1:p.His1380Asp
XM_017017791.1:c.4138C>G	XP_016873280.1:p.His1380Asp
XM_017017792.2:c.4138C>G	XP_016873281.1:p.His1380Asp
XR_002957150.1:n.4871C>G
NM_001351834.2:c.4138C>G	NP_001338763.1:p.His1380Asp
NM_000051.4:c.4138C>G MANE Select	NP_000042.3:p.His1380Asp