Canonical Allele Identifier: CA1998803655

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108307910T= , CM000673.2:g.108307910T=	GRCh38
NC_000011.9:g.108178637T= , CM000673.1:g.108178637T=	GRCh37
NC_000011.8:g.107683847T=	NCBI36
NG_009830.1:g.90079T= , LRG_135:g.90079T=
NG_054724.1:g.166923A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5688T=	ENSP00000388058.2:p.Phe1896=
ENST00000713593.1:c.*5159T=	ENSP00000518889.1:n.*5159T=
ENST00000278616.9:c.5688T=	ENSP00000278616.4:p.Phe1896=
ENST00000525056.2:n.107T=
ENST00000682286.1:n.445T=
ENST00000682302.1:n.106T=
ENST00000683174.1:n.7172T=
ENST00000683524.1:n.912T=
ENST00000684152.1:n.1402T=
ENST00000527805.6:c.*752T=	ENSP00000435747.2:n.*752T=
ENST00000675595.1:c.*752T=	ENSP00000502563.1:n.*752T=
ENST00000675843.1:c.5688T= MANE Select	ENSP00000501606.1:p.Phe1896=
ENST00000278616.8:c.5688T=	ENSP00000278616.4:p.Phe1896=
ENST00000452508.6:c.5688T=	ENSP00000388058.2:p.Phe1896=
ENST00000524792.5:n.1903T=
ENST00000529588.5:c.187-2250T=
ENST00000533690.5:n.1092T=
NM_000051.3:c.5688T= , LRG_135t1:c.5688T=	NP_000042.3:p.Phe1896=
XM_005271561.3:c.5688T=	XP_005271618.2:p.Phe1896=
XM_005271562.3:c.5688T=	XP_005271619.2:p.Phe1896=
XM_006718843.2:c.5688T=	XP_006718906.1:p.Phe1896=
XM_006718845.1:c.1644T=	XP_006718908.1:p.Phe548=
XM_011542840.1:c.5688T=	XP_011541142.1:p.Phe1896=
XM_011542841.1:c.5688T=	XP_011541143.1:p.Phe1896=
XM_011542842.1:c.5523T=	XP_011541144.1:p.Phe1841=
XM_011542843.1:c.5688T=	XP_011541145.1:p.Phe1896=
XM_011542844.1:c.4644T=	XP_011541146.1:p.Phe1548=
XM_011542845.1:c.4380T=	XP_011541147.1:p.Phe1460=
XM_011542847.1:c.759T=	XP_011541149.1:p.Phe253=
NM_001351834.1:c.5688T=	NP_001338763.1:p.Phe1896=
XM_005271562.5:c.5688T=	XP_005271619.2:p.Phe1896=
XM_006718843.4:c.5688T=	XP_006718906.1:p.Phe1896=
XM_006718845.2:c.1644T=	XP_006718908.1:p.Phe548=
XM_011542840.3:c.5688T=	XP_011541142.1:p.Phe1896=
XM_011542842.3:c.5523T=	XP_011541144.1:p.Phe1841=
XM_011542843.2:c.5688T=	XP_011541145.1:p.Phe1896=
XM_011542844.3:c.4644T=	XP_011541146.1:p.Phe1548=
XM_011542845.2:c.4380T=	XP_011541147.1:p.Phe1460=
XM_017017789.2:c.5688T=	XP_016873278.1:p.Phe1896=
XM_017017790.2:c.5688T=	XP_016873279.1:p.Phe1896=
XM_017017791.1:c.5688T=	XP_016873280.1:p.Phe1896=
XR_002957150.1:n.6288T=
NM_001351834.2:c.5688T=	NP_001338763.1:p.Phe1896=
NM_000051.4:c.5688T= MANE Select	NP_000042.3:p.Phe1896=