Canonical Allele Identifier: CA10584352

Gene: ATM

Linked Data

• ClinVar Variation Id: 246068
• ClinVar RCV Id: RCV000236378 ; RCV000628037 ; RCV002347925 ; RCV004020927
• dbSNP Id: rs879254076
• MyVariant Identifiers: chr11:g.108175478G>A (hg19) ; chr11:g.108304751G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108304751G>A , CM000673.2:g.108304751G>A	GRCh38
NC_000011.9:g.108175478G>A , CM000673.1:g.108175478G>A	GRCh37
NC_000011.8:g.107680688G>A	NCBI36
NG_009830.1:g.86920G>A , LRG_135:g.86920G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5573G>A	ENSP00000388058.2:p.Trp1858Ter
ENST00000713593.1:c.*5044G>A	ENSP00000518889.1:n.*5044G>A
ENST00000278616.9:c.5573G>A	ENSP00000278616.4:p.Trp1858Ter
ENST00000683174.1:n.7057G>A
ENST00000683524.1:n.797G>A
ENST00000684152.1:n.1287G>A
ENST00000527805.6:c.*637G>A	ENSP00000435747.2:n.*637G>A
ENST00000675595.1:c.*637G>A	ENSP00000502563.1:n.*637G>A
ENST00000675843.1:c.5573G>A MANE Select	ENSP00000501606.1:p.Trp1858Ter
ENST00000278616.8:c.5573G>A	ENSP00000278616.4:p.Trp1858Ter
ENST00000452508.6:c.5573G>A	ENSP00000388058.2:p.Trp1858Ter
ENST00000524792.5:n.1788G>A
ENST00000529588.5:c.85G>A
ENST00000533690.5:n.977G>A
NM_000051.3:c.5573G>A , LRG_135t1:c.5573G>A	NP_000042.3:p.Trp1858Ter
XM_005271561.3:c.5573G>A	XP_005271618.2:p.Trp1858Ter
XM_005271562.3:c.5573G>A	XP_005271619.2:p.Trp1858Ter
XM_006718843.2:c.5573G>A	XP_006718906.1:p.Trp1858Ter
XM_006718845.1:c.1529G>A	XP_006718908.1:p.Trp510Ter
XM_011542840.1:c.5573G>A	XP_011541142.1:p.Trp1858Ter
XM_011542841.1:c.5573G>A	XP_011541143.1:p.Trp1858Ter
XM_011542842.1:c.5408G>A	XP_011541144.1:p.Trp1803Ter
XM_011542843.1:c.5573G>A	XP_011541145.1:p.Trp1858Ter
XM_011542844.1:c.4529G>A	XP_011541146.1:p.Trp1510Ter
XM_011542845.1:c.4265G>A	XP_011541147.1:p.Trp1422Ter
XM_011542847.1:c.644G>A	XP_011541149.1:p.Trp215Ter
NM_001351834.1:c.5573G>A	NP_001338763.1:p.Trp1858Ter
XM_005271562.5:c.5573G>A	XP_005271619.2:p.Trp1858Ter
XM_006718843.4:c.5573G>A	XP_006718906.1:p.Trp1858Ter
XM_006718845.2:c.1529G>A	XP_006718908.1:p.Trp510Ter
XM_011542840.3:c.5573G>A	XP_011541142.1:p.Trp1858Ter
XM_011542842.3:c.5408G>A	XP_011541144.1:p.Trp1803Ter
XM_011542843.2:c.5573G>A	XP_011541145.1:p.Trp1858Ter
XM_011542844.3:c.4529G>A	XP_011541146.1:p.Trp1510Ter
XM_011542845.2:c.4265G>A	XP_011541147.1:p.Trp1422Ter
XM_017017789.2:c.5573G>A	XP_016873278.1:p.Trp1858Ter
XM_017017790.2:c.5573G>A	XP_016873279.1:p.Trp1858Ter
XM_017017791.1:c.5573G>A	XP_016873280.1:p.Trp1858Ter
XR_002957150.1:n.6173G>A
NM_001351834.2:c.5573G>A	NP_001338763.1:p.Trp1858Ter
NM_000051.4:c.5573G>A MANE Select	NP_000042.3:p.Trp1858Ter