Canonical Allele Identifier: CA1998757938

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108223008T= , CM000673.2:g.108223008T=	GRCh38
NC_000011.9:g.108093735T= , CM000673.1:g.108093735T=	GRCh37
NC_000011.8:g.107598945T=	NCBI36
NG_009830.1:g.5177T= , LRG_135:g.5177T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.-297T=	ENSP00000388058.2:n.-297T=
ENST00000683914.2:c.-209T=	ENSP00000507649.1:n.-209T=
ENST00000278616.8:c.-209T=	ENSP00000278616.4:n.-209T=
ENST00000527805.5:c.-209T=	ENSP00000435747.1:n.-209T=
NM_000051.3:c.-209T= , LRG_135t1:c.-209T=	NP_000042.3:n.-209T=
XM_011542843.1:c.-209T=	XP_011541145.1:n.-209T=
XM_011542846.1:c.-209T=	XP_011541148.1:n.-209T=
NM_001351834.1:c.-297T=	NP_001338763.1:n.-297T=
NM_001351835.1:c.-209T=	NP_001338764.1:n.-209T=
XM_011542842.3:c.-209T=	XP_011541144.1:n.-209T=
XM_011542843.2:c.-209T=	XP_011541145.1:n.-209T=
XM_011542844.3:c.-1231T=	XP_011541146.1:n.-1231T=
XM_017017791.1:c.-209T=	XP_016873280.1:n.-209T=
XM_017017792.2:c.-209T=	XP_016873281.1:n.-209T=
XR_002957150.1:n.525T=