Canonical Allele Identifier: CA1998758098

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108223136C= , CM000673.2:g.108223136C=	GRCh38
NC_000011.9:g.108093863C= , CM000673.1:g.108093863C=	GRCh37
NC_000011.8:g.107599073C=	NCBI36
NG_009830.1:g.5305C= , LRG_135:g.5305C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.-169C=	ENSP00000388058.2:n.-169C=
ENST00000683914.2:c.-81C=	ENSP00000507649.1:n.-81C=
ENST00000713593.1:c.-81C=	ENSP00000518889.1:n.-81C=
ENST00000683174.1:n.70C=
ENST00000683468.1:c.-4489C=	ENSP00000508178.1:n.-4489C=
ENST00000683488.1:n.93C=
ENST00000527805.6:c.-81C=	ENSP00000435747.2:n.-81C=
ENST00000675595.1:c.-81C=	ENSP00000502563.1:n.-81C=
ENST00000675843.1:c.-81C= MANE Select	ENSP00000501606.1:n.-81C=
ENST00000278616.8:c.-81C=	ENSP00000278616.4:n.-81C=
ENST00000452508.6:c.-169C=	ENSP00000388058.2:n.-169C=
ENST00000527805.5:c.-81C=	ENSP00000435747.1:n.-81C=
ENST00000527891.5:c.-81C=	ENSP00000433955.1:n.-81C=
ENST00000530958.5:c.-4489C=	ENSP00000483338.1:n.-4489C=
ENST00000532931.5:c.-155C=	ENSP00000432318.1:n.-155C=
NM_000051.3:c.-81C= , LRG_135t1:c.-81C=	NP_000042.3:n.-81C=
XM_005271561.3:c.-169C=	XP_005271618.2:n.-169C=
XM_011542841.1:c.-872C=	XP_011541143.1:n.-872C=
XM_011542842.1:c.-81C=	XP_011541144.1:n.-81C=
XM_011542843.1:c.-81C=	XP_011541145.1:n.-81C=
XM_011542846.1:c.-81C=	XP_011541148.1:n.-81C=
NM_001351834.1:c.-169C=	NP_001338763.1:n.-169C=
NM_001351835.1:c.-81C=	NP_001338764.1:n.-81C=
XM_011542842.3:c.-81C=	XP_011541144.1:n.-81C=
XM_011542843.2:c.-81C=	XP_011541145.1:n.-81C=
XM_011542844.3:c.-1103C=	XP_011541146.1:n.-1103C=
XM_017017791.1:c.-81C=	XP_016873280.1:n.-81C=
XM_017017792.2:c.-81C=	XP_016873281.1:n.-81C=
XR_002957150.1:n.653C=
NM_001351834.2:c.-169C=	NP_001338763.1:n.-169C=
NM_000051.4:c.-81C= MANE Select	NP_000042.3:n.-81C=
NM_001351835.2:c.-81C=	NP_001338764.1:n.-81C=