Canonical Allele Identifier: CA1998785588

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108289752T= , CM000673.2:g.108289752T=	GRCh38
NC_000011.9:g.108160479T= , CM000673.1:g.108160479T=	GRCh37
NC_000011.8:g.107665689T=	NCBI36
NG_009830.1:g.71921T= , LRG_135:g.71921T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.4387T=	ENSP00000388058.2:p.Phe1463=
ENST00000713593.1:c.*3858T=	ENSP00000518889.1:n.*3858T=
ENST00000278616.9:c.4387T=	ENSP00000278616.4:p.Phe1463=
ENST00000533733.6:n.1650T=
ENST00000683174.1:n.4537T=
ENST00000527805.6:c.4387T=	ENSP00000435747.2:p.Phe1463=
ENST00000675595.1:c.4222T=	ENSP00000502563.1:p.Phe1408=
ENST00000675843.1:c.4387T= MANE Select	ENSP00000501606.1:p.Phe1463=
ENST00000278616.8:c.4387T=	ENSP00000278616.4:p.Phe1463=
ENST00000452508.6:c.4387T=	ENSP00000388058.2:p.Phe1463=
ENST00000524792.5:n.602T=
ENST00000531525.2:c.394T=	ENSP00000434327.2:p.Phe132=
ENST00000533733.5:n.816T=
NM_000051.3:c.4387T= , LRG_135t1:c.4387T=	NP_000042.3:p.Phe1463=
XM_005271561.3:c.4387T=	XP_005271618.2:p.Phe1463=
XM_005271562.3:c.4387T=	XP_005271619.2:p.Phe1463=
XM_006718843.2:c.4387T=	XP_006718906.1:p.Phe1463=
XM_006718845.1:c.343T=	XP_006718908.1:p.Phe115=
XM_011542840.1:c.4387T=	XP_011541142.1:p.Phe1463=
XM_011542841.1:c.4387T=	XP_011541143.1:p.Phe1463=
XM_011542842.1:c.4222T=	XP_011541144.1:p.Phe1408=
XM_011542843.1:c.4387T=	XP_011541145.1:p.Phe1463=
XM_011542844.1:c.3343T=	XP_011541146.1:p.Phe1115=
XM_011542845.1:c.3079T=	XP_011541147.1:p.Phe1027=
XM_011542846.1:c.4387T=	XP_011541148.1:p.Phe1463=
NM_001351834.1:c.4387T=	NP_001338763.1:p.Phe1463=
XM_005271562.5:c.4387T=	XP_005271619.2:p.Phe1463=
XM_006718843.4:c.4387T=	XP_006718906.1:p.Phe1463=
XM_006718845.2:c.343T=	XP_006718908.1:p.Phe115=
XM_011542840.3:c.4387T=	XP_011541142.1:p.Phe1463=
XM_011542842.3:c.4222T=	XP_011541144.1:p.Phe1408=
XM_011542843.2:c.4387T=	XP_011541145.1:p.Phe1463=
XM_011542844.3:c.3343T=	XP_011541146.1:p.Phe1115=
XM_011542845.2:c.3079T=	XP_011541147.1:p.Phe1027=
XM_017017789.2:c.4387T=	XP_016873278.1:p.Phe1463=
XM_017017790.2:c.4387T=	XP_016873279.1:p.Phe1463=
XM_017017791.1:c.4387T=	XP_016873280.1:p.Phe1463=
XM_017017792.2:c.4387T=	XP_016873281.1:p.Phe1463=
XR_002957150.1:n.5120T=
NM_001351834.2:c.4387T=	NP_001338763.1:p.Phe1463=
NM_000051.4:c.4387T= MANE Select	NP_000042.3:p.Phe1463=