Canonical Allele Identifier: CA382535407

Gene: ATM

Linked Data

• dbSNP Id: rs879254227
• gnomAD v2: 11-108122715-G-T
• MyVariant Identifiers: chr11:g.108122715G>T (hg19) ; chr11:g.108251988G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108251988G>T , CM000673.2:g.108251988G>T	GRCh38
NC_000011.9:g.108122715G>T , CM000673.1:g.108122715G>T	GRCh37
NC_000011.8:g.107627925G>T	NCBI36
NG_009830.1:g.34157G>T , LRG_135:g.34157G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.1759G>T	ENSP00000388058.2:p.Gly587Cys
ENST00000713593.1:c.*1230G>T	ENSP00000518889.1:n.*1230G>T
ENST00000278616.9:c.1759G>T	ENSP00000278616.4:p.Gly587Cys
ENST00000682516.1:n.1893G>T
ENST00000683174.1:n.1909G>T
ENST00000683605.1:n.1254G>T
ENST00000684037.1:c.*694G>T	ENSP00000508245.1:n.*694G>T
ENST00000684061.1:n.1893G>T
ENST00000527805.6:c.1759G>T	ENSP00000435747.2:p.Gly587Cys
ENST00000675595.1:c.1594G>T	ENSP00000502563.1:p.Gly532Cys
ENST00000675843.1:c.1759G>T MANE Select	ENSP00000501606.1:p.Gly587Cys
ENST00000278616.8:c.1759G>T	ENSP00000278616.4:p.Gly587Cys
ENST00000452508.6:c.1759G>T	ENSP00000388058.2:p.Gly587Cys
ENST00000527805.5:c.1759G>T	ENSP00000435747.1:p.Gly587Cys
NM_000051.3:c.1759G>T , LRG_135t1:c.1759G>T	NP_000042.3:p.Gly587Cys
XM_005271561.3:c.1759G>T	XP_005271618.2:p.Gly587Cys
XM_005271562.3:c.1759G>T	XP_005271619.2:p.Gly587Cys
XM_006718843.2:c.1759G>T	XP_006718906.1:p.Gly587Cys
XM_011542840.1:c.1759G>T	XP_011541142.1:p.Gly587Cys
XM_011542841.1:c.1759G>T	XP_011541143.1:p.Gly587Cys
XM_011542842.1:c.1594G>T	XP_011541144.1:p.Gly532Cys
XM_011542843.1:c.1759G>T	XP_011541145.1:p.Gly587Cys
XM_011542844.1:c.715G>T	XP_011541146.1:p.Gly239Cys
XM_011542845.1:c.451G>T	XP_011541147.1:p.Gly151Cys
XM_011542846.1:c.1759G>T	XP_011541148.1:p.Gly587Cys
NM_001351834.1:c.1759G>T	NP_001338763.1:p.Gly587Cys
XM_005271562.5:c.1759G>T	XP_005271619.2:p.Gly587Cys
XM_006718843.4:c.1759G>T	XP_006718906.1:p.Gly587Cys
XM_011542840.3:c.1759G>T	XP_011541142.1:p.Gly587Cys
XM_011542842.3:c.1594G>T	XP_011541144.1:p.Gly532Cys
XM_011542843.2:c.1759G>T	XP_011541145.1:p.Gly587Cys
XM_011542844.3:c.715G>T	XP_011541146.1:p.Gly239Cys
XM_011542845.2:c.451G>T	XP_011541147.1:p.Gly151Cys
XM_017017789.2:c.1759G>T	XP_016873278.1:p.Gly587Cys
XM_017017790.2:c.1759G>T	XP_016873279.1:p.Gly587Cys
XM_017017791.1:c.1759G>T	XP_016873280.1:p.Gly587Cys
XM_017017792.2:c.1759G>T	XP_016873281.1:p.Gly587Cys
XR_002957150.1:n.2492G>T
NM_001351834.2:c.1759G>T	NP_001338763.1:p.Gly587Cys
NM_000051.4:c.1759G>T MANE Select	NP_000042.3:p.Gly587Cys