Canonical Allele Identifier: CA6265759

Gene: ATM

Linked Data

• ClinVar Variation Id: 421488
• ClinVar RCV Id: RCV000478233 ; RCV001045999 ; RCV002350067 ; RCV004023152
• dbSNP Id: rs753839301
• ExAC: 11:108178646 C / A
• COSMIC: COSM5024999 ; COSM5025000
• MyVariant Identifiers: chr11:g.108178646C>A (hg19) ; chr11:g.108307919C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108307919C>A , CM000673.2:g.108307919C>A	GRCh38
NC_000011.9:g.108178646C>A , CM000673.1:g.108178646C>A	GRCh37
NC_000011.8:g.107683856C>A	NCBI36
NG_009830.1:g.90088C>A , LRG_135:g.90088C>A
NG_054724.1:g.166914G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5697C>A	ENSP00000388058.2:p.Cys1899Ter
ENST00000713593.1:c.*5168C>A	ENSP00000518889.1:n.*5168C>A
ENST00000278616.9:c.5697C>A	ENSP00000278616.4:p.Cys1899Ter
ENST00000525056.2:n.116C>A
ENST00000682286.1:n.454C>A
ENST00000682302.1:n.115C>A
ENST00000683174.1:n.7181C>A
ENST00000683524.1:n.921C>A
ENST00000684152.1:n.1411C>A
ENST00000527805.6:c.*761C>A	ENSP00000435747.2:n.*761C>A
ENST00000675595.1:c.*761C>A	ENSP00000502563.1:n.*761C>A
ENST00000675843.1:c.5697C>A MANE Select	ENSP00000501606.1:p.Cys1899Ter
ENST00000278616.8:c.5697C>A	ENSP00000278616.4:p.Cys1899Ter
ENST00000452508.6:c.5697C>A	ENSP00000388058.2:p.Cys1899Ter
ENST00000524792.5:n.1912C>A
ENST00000529588.5:c.187-2241C>A
ENST00000533690.5:n.1101C>A
NM_000051.3:c.5697C>A , LRG_135t1:c.5697C>A	NP_000042.3:p.Cys1899Ter
XM_005271561.3:c.5697C>A	XP_005271618.2:p.Cys1899Ter
XM_005271562.3:c.5697C>A	XP_005271619.2:p.Cys1899Ter
XM_006718843.2:c.5697C>A	XP_006718906.1:p.Cys1899Ter
XM_006718845.1:c.1653C>A	XP_006718908.1:p.Cys551Ter
XM_011542840.1:c.5697C>A	XP_011541142.1:p.Cys1899Ter
XM_011542841.1:c.5697C>A	XP_011541143.1:p.Cys1899Ter
XM_011542842.1:c.5532C>A	XP_011541144.1:p.Cys1844Ter
XM_011542843.1:c.5697C>A	XP_011541145.1:p.Cys1899Ter
XM_011542844.1:c.4653C>A	XP_011541146.1:p.Cys1551Ter
XM_011542845.1:c.4389C>A	XP_011541147.1:p.Cys1463Ter
XM_011542847.1:c.768C>A	XP_011541149.1:p.Cys256Ter
NM_001351834.1:c.5697C>A	NP_001338763.1:p.Cys1899Ter
XM_005271562.5:c.5697C>A	XP_005271619.2:p.Cys1899Ter
XM_006718843.4:c.5697C>A	XP_006718906.1:p.Cys1899Ter
XM_006718845.2:c.1653C>A	XP_006718908.1:p.Cys551Ter
XM_011542840.3:c.5697C>A	XP_011541142.1:p.Cys1899Ter
XM_011542842.3:c.5532C>A	XP_011541144.1:p.Cys1844Ter
XM_011542843.2:c.5697C>A	XP_011541145.1:p.Cys1899Ter
XM_011542844.3:c.4653C>A	XP_011541146.1:p.Cys1551Ter
XM_011542845.2:c.4389C>A	XP_011541147.1:p.Cys1463Ter
XM_017017789.2:c.5697C>A	XP_016873278.1:p.Cys1899Ter
XM_017017790.2:c.5697C>A	XP_016873279.1:p.Cys1899Ter
XM_017017791.1:c.5697C>A	XP_016873280.1:p.Cys1899Ter
XR_002957150.1:n.6297C>A
NM_001351834.2:c.5697C>A	NP_001338763.1:p.Cys1899Ter
NM_000051.4:c.5697C>A MANE Select	NP_000042.3:p.Cys1899Ter