Canonical Allele Identifier: CA382532094

Gene: ATM

Linked Data

• ClinVar Variation Id: 1449085
• ClinVar RCV Id: RCV002012313
• dbSNP Id: rs2135764207
• MyVariant Identifiers: chr11:g.108160464G>A (hg19) ; chr11:g.108289737G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108289737G>A , CM000673.2:g.108289737G>A	GRCh38
NC_000011.9:g.108160464G>A , CM000673.1:g.108160464G>A	GRCh37
NC_000011.8:g.107665674G>A	NCBI36
NG_009830.1:g.71906G>A , LRG_135:g.71906G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.4372G>A	ENSP00000388058.2:p.Gly1458Arg
ENST00000713593.1:c.*3843G>A	ENSP00000518889.1:n.*3843G>A
ENST00000278616.9:c.4372G>A	ENSP00000278616.4:p.Gly1458Arg
ENST00000533733.6:n.1635G>A
ENST00000683174.1:n.4522G>A
ENST00000527805.6:c.4372G>A	ENSP00000435747.2:p.Gly1458Arg
ENST00000675595.1:c.4207G>A	ENSP00000502563.1:p.Gly1403Arg
ENST00000675843.1:c.4372G>A MANE Select	ENSP00000501606.1:p.Gly1458Arg
ENST00000278616.8:c.4372G>A	ENSP00000278616.4:p.Gly1458Arg
ENST00000452508.6:c.4372G>A	ENSP00000388058.2:p.Gly1458Arg
ENST00000524792.5:n.587G>A
ENST00000531525.2:c.379G>A	ENSP00000434327.2:p.Gly127Arg
ENST00000533733.5:n.801G>A
NM_000051.3:c.4372G>A , LRG_135t1:c.4372G>A	NP_000042.3:p.Gly1458Arg
XM_005271561.3:c.4372G>A	XP_005271618.2:p.Gly1458Arg
XM_005271562.3:c.4372G>A	XP_005271619.2:p.Gly1458Arg
XM_006718843.2:c.4372G>A	XP_006718906.1:p.Gly1458Arg
XM_006718845.1:c.328G>A	XP_006718908.1:p.Gly110Arg
XM_011542840.1:c.4372G>A	XP_011541142.1:p.Gly1458Arg
XM_011542841.1:c.4372G>A	XP_011541143.1:p.Gly1458Arg
XM_011542842.1:c.4207G>A	XP_011541144.1:p.Gly1403Arg
XM_011542843.1:c.4372G>A	XP_011541145.1:p.Gly1458Arg
XM_011542844.1:c.3328G>A	XP_011541146.1:p.Gly1110Arg
XM_011542845.1:c.3064G>A	XP_011541147.1:p.Gly1022Arg
XM_011542846.1:c.4372G>A	XP_011541148.1:p.Gly1458Arg
NM_001351834.1:c.4372G>A	NP_001338763.1:p.Gly1458Arg
XM_005271562.5:c.4372G>A	XP_005271619.2:p.Gly1458Arg
XM_006718843.4:c.4372G>A	XP_006718906.1:p.Gly1458Arg
XM_006718845.2:c.328G>A	XP_006718908.1:p.Gly110Arg
XM_011542840.3:c.4372G>A	XP_011541142.1:p.Gly1458Arg
XM_011542842.3:c.4207G>A	XP_011541144.1:p.Gly1403Arg
XM_011542843.2:c.4372G>A	XP_011541145.1:p.Gly1458Arg
XM_011542844.3:c.3328G>A	XP_011541146.1:p.Gly1110Arg
XM_011542845.2:c.3064G>A	XP_011541147.1:p.Gly1022Arg
XM_017017789.2:c.4372G>A	XP_016873278.1:p.Gly1458Arg
XM_017017790.2:c.4372G>A	XP_016873279.1:p.Gly1458Arg
XM_017017791.1:c.4372G>A	XP_016873280.1:p.Gly1458Arg
XM_017017792.2:c.4372G>A	XP_016873281.1:p.Gly1458Arg
XR_002957150.1:n.5105G>A
NM_001351834.2:c.4372G>A	NP_001338763.1:p.Gly1458Arg
NM_000051.4:c.4372G>A MANE Select	NP_000042.3:p.Gly1458Arg