Canonical Allele Identifier: CA1998758065

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108223108G= , CM000673.2:g.108223108G=	GRCh38
NC_000011.9:g.108093835G= , CM000673.1:g.108093835G=	GRCh37
NC_000011.8:g.107599045G=	NCBI36
NG_009830.1:g.5277G= , LRG_135:g.5277G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.-197G=	ENSP00000388058.2:n.-197G=
ENST00000683914.2:c.-109G=	ENSP00000507649.1:n.-109G=
ENST00000713593.1:c.-109G=	ENSP00000518889.1:n.-109G=
ENST00000683174.1:n.42G=
ENST00000683468.1:c.-4517G=	ENSP00000508178.1:n.-4517G=
ENST00000683488.1:n.65G=
ENST00000527805.6:c.-109G=	ENSP00000435747.2:n.-109G=
ENST00000675595.1:c.-109G=	ENSP00000502563.1:n.-109G=
ENST00000675843.1:c.-109G= MANE Select	ENSP00000501606.1:n.-109G=
ENST00000278616.8:c.-109G=	ENSP00000278616.4:n.-109G=
ENST00000527805.5:c.-109G=	ENSP00000435747.1:n.-109G=
ENST00000527891.5:c.-109G=	ENSP00000433955.1:n.-109G=
ENST00000530958.5:c.-4517G=	ENSP00000483338.1:n.-4517G=
ENST00000532931.5:c.-183G=	ENSP00000432318.1:n.-183G=
NM_000051.3:c.-109G= , LRG_135t1:c.-109G=	NP_000042.3:n.-109G=
XM_005271561.3:c.-197G=	XP_005271618.2:n.-197G=
XM_011542841.1:c.-900G=	XP_011541143.1:n.-900G=
XM_011542842.1:c.-109G=	XP_011541144.1:n.-109G=
XM_011542843.1:c.-109G=	XP_011541145.1:n.-109G=
XM_011542846.1:c.-109G=	XP_011541148.1:n.-109G=
NM_001351834.1:c.-197G=	NP_001338763.1:n.-197G=
NM_001351835.1:c.-109G=	NP_001338764.1:n.-109G=
XM_011542842.3:c.-109G=	XP_011541144.1:n.-109G=
XM_011542843.2:c.-109G=	XP_011541145.1:n.-109G=
XM_011542844.3:c.-1131G=	XP_011541146.1:n.-1131G=
XM_017017791.1:c.-109G=	XP_016873280.1:n.-109G=
XM_017017792.2:c.-109G=	XP_016873281.1:n.-109G=
XR_002957150.1:n.625G=
NM_001351834.2:c.-197G=	NP_001338763.1:n.-197G=
NM_000051.4:c.-109G= MANE Select	NP_000042.3:n.-109G=
NM_001351835.2:c.-109G=	NP_001338764.1:n.-109G=