Canonical Allele Identifier: CA1998803652

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108307907C= , CM000673.2:g.108307907C=	GRCh38
NC_000011.9:g.108178634C= , CM000673.1:g.108178634C=	GRCh37
NC_000011.8:g.107683844C=	NCBI36
NG_009830.1:g.90076C= , LRG_135:g.90076C=
NG_054724.1:g.166926G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5685C=	ENSP00000388058.2:p.His1895=
ENST00000713593.1:c.*5156C=	ENSP00000518889.1:n.*5156C=
ENST00000278616.9:c.5685C=	ENSP00000278616.4:p.His1895=
ENST00000525056.2:n.104C=
ENST00000682286.1:n.442C=
ENST00000682302.1:n.103C=
ENST00000683174.1:n.7169C=
ENST00000683524.1:n.909C=
ENST00000684152.1:n.1399C=
ENST00000527805.6:c.*749C=	ENSP00000435747.2:n.*749C=
ENST00000675595.1:c.*749C=	ENSP00000502563.1:n.*749C=
ENST00000675843.1:c.5685C= MANE Select	ENSP00000501606.1:p.His1895=
ENST00000278616.8:c.5685C=	ENSP00000278616.4:p.His1895=
ENST00000452508.6:c.5685C=	ENSP00000388058.2:p.His1895=
ENST00000524792.5:n.1900C=
ENST00000529588.5:c.187-2253C=
ENST00000533690.5:n.1089C=
NM_000051.3:c.5685C= , LRG_135t1:c.5685C=	NP_000042.3:p.His1895=
XM_005271561.3:c.5685C=	XP_005271618.2:p.His1895=
XM_005271562.3:c.5685C=	XP_005271619.2:p.His1895=
XM_006718843.2:c.5685C=	XP_006718906.1:p.His1895=
XM_006718845.1:c.1641C=	XP_006718908.1:p.His547=
XM_011542840.1:c.5685C=	XP_011541142.1:p.His1895=
XM_011542841.1:c.5685C=	XP_011541143.1:p.His1895=
XM_011542842.1:c.5520C=	XP_011541144.1:p.His1840=
XM_011542843.1:c.5685C=	XP_011541145.1:p.His1895=
XM_011542844.1:c.4641C=	XP_011541146.1:p.His1547=
XM_011542845.1:c.4377C=	XP_011541147.1:p.His1459=
XM_011542847.1:c.756C=	XP_011541149.1:p.His252=
NM_001351834.1:c.5685C=	NP_001338763.1:p.His1895=
XM_005271562.5:c.5685C=	XP_005271619.2:p.His1895=
XM_006718843.4:c.5685C=	XP_006718906.1:p.His1895=
XM_006718845.2:c.1641C=	XP_006718908.1:p.His547=
XM_011542840.3:c.5685C=	XP_011541142.1:p.His1895=
XM_011542842.3:c.5520C=	XP_011541144.1:p.His1840=
XM_011542843.2:c.5685C=	XP_011541145.1:p.His1895=
XM_011542844.3:c.4641C=	XP_011541146.1:p.His1547=
XM_011542845.2:c.4377C=	XP_011541147.1:p.His1459=
XM_017017789.2:c.5685C=	XP_016873278.1:p.His1895=
XM_017017790.2:c.5685C=	XP_016873279.1:p.His1895=
XM_017017791.1:c.5685C=	XP_016873280.1:p.His1895=
XR_002957150.1:n.6285C=
NM_001351834.2:c.5685C=	NP_001338763.1:p.His1895=
NM_000051.4:c.5685C= MANE Select	NP_000042.3:p.His1895=