Canonical Allele Identifier: CA1998758019

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108223076C= , CM000673.2:g.108223076C=	GRCh38
NC_000011.9:g.108093803C= , CM000673.1:g.108093803C=	GRCh37
NC_000011.8:g.107599013C=	NCBI36
NG_009830.1:g.5245C= , LRG_135:g.5245C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.-229C=	ENSP00000388058.2:n.-229C=
ENST00000683914.2:c.-141C=	ENSP00000507649.1:n.-141C=
ENST00000713593.1:c.-141C=	ENSP00000518889.1:n.-141C=
ENST00000683174.1:n.10C=
ENST00000683488.1:n.33C=
ENST00000527805.6:c.-141C=	ENSP00000435747.2:n.-141C=
ENST00000675843.1:c.-141C= MANE Select	ENSP00000501606.1:n.-141C=
ENST00000278616.8:c.-141C=	ENSP00000278616.4:n.-141C=
ENST00000527805.5:c.-141C=	ENSP00000435747.1:n.-141C=
NM_000051.3:c.-141C= , LRG_135t1:c.-141C=	NP_000042.3:n.-141C=
XM_011542843.1:c.-141C=	XP_011541145.1:n.-141C=
XM_011542846.1:c.-141C=	XP_011541148.1:n.-141C=
NM_001351834.1:c.-229C=	NP_001338763.1:n.-229C=
NM_001351835.1:c.-141C=	NP_001338764.1:n.-141C=
XM_011542842.3:c.-141C=	XP_011541144.1:n.-141C=
XM_011542843.2:c.-141C=	XP_011541145.1:n.-141C=
XM_011542844.3:c.-1163C=	XP_011541146.1:n.-1163C=
XM_017017791.1:c.-141C=	XP_016873280.1:n.-141C=
XM_017017792.2:c.-141C=	XP_016873281.1:n.-141C=
XR_002957150.1:n.593C=
NM_001351834.2:c.-229C=	NP_001338763.1:n.-229C=
NM_000051.4:c.-141C= MANE Select	NP_000042.3:n.-141C=
NM_001351835.2:c.-141C=	NP_001338764.1:n.-141C=