Canonical Allele Identifier: CA1998772546

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108268586_108268587delinsAC , CM000673.2:g.108268586_108268587delinsAC	GRCh38
NC_000011.9:g.108139313_108139314delinsAC , CM000673.1:g.108139313_108139314delinsAC	GRCh37
NC_000011.8:g.107644523_107644524delinsAC	NCBI36
NG_009830.1:g.50755_50756delinsAC , LRG_135:g.50755_50756delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.2815_2816delinsAC	ENSP00000388058.2:p.Thr939=
ENST00000713593.1:c.*2286_*2287delinsAC	ENSP00000518889.1:n.*2286_*2287delinsAC
ENST00000278616.9:c.2815_2816delinsAC	ENSP00000278616.4:p.Thr939=
ENST00000682516.1:n.2772+1244_2772+1245delinsAC
ENST00000683174.1:n.2965_2966delinsAC
ENST00000684037.1:c.*1573+1244_*1573+1245delinsAC	ENSP00000508245.1:n.*1573+1244_*1573+1245delinsAC
ENST00000527805.6:c.2815_2816delinsAC	ENSP00000435747.2:p.Thr939=
ENST00000675595.1:c.2650_2651delinsAC	ENSP00000502563.1:p.Thr884=
ENST00000675843.1:c.2815_2816delinsAC MANE Select	ENSP00000501606.1:p.Thr939=
ENST00000278616.8:c.2815_2816delinsAC	ENSP00000278616.4:p.Thr939=
ENST00000419286.2:n.177_178delinsAC
ENST00000452508.6:c.2815_2816delinsAC	ENSP00000388058.2:p.Thr939=
ENST00000527805.5:c.2815_2816delinsAC	ENSP00000435747.1:p.Thr939=
NM_000051.3:c.2815_2816delinsAC , LRG_135t1:c.2815_2816delinsAC	NP_000042.3:p.Thr939=
XM_005271561.3:c.2815_2816delinsAC	XP_005271618.2:p.Thr939=
XM_005271562.3:c.2815_2816delinsAC	XP_005271619.2:p.Thr939=
XM_006718843.2:c.2815_2816delinsAC	XP_006718906.1:p.Thr939=
XM_011542840.1:c.2815_2816delinsAC	XP_011541142.1:p.Thr939=
XM_011542841.1:c.2815_2816delinsAC	XP_011541143.1:p.Thr939=
XM_011542842.1:c.2650_2651delinsAC	XP_011541144.1:p.Thr884=
XM_011542843.1:c.2815_2816delinsAC	XP_011541145.1:p.Thr939=
XM_011542844.1:c.1771_1772delinsAC	XP_011541146.1:p.Thr591=
XM_011542845.1:c.1507_1508delinsAC	XP_011541147.1:p.Thr503=
XM_011542846.1:c.2815_2816delinsAC	XP_011541148.1:p.Thr939=
NM_001351834.1:c.2815_2816delinsAC	NP_001338763.1:p.Thr939=
XM_005271562.5:c.2815_2816delinsAC	XP_005271619.2:p.Thr939=
XM_006718843.4:c.2815_2816delinsAC	XP_006718906.1:p.Thr939=
XM_011542840.3:c.2815_2816delinsAC	XP_011541142.1:p.Thr939=
XM_011542842.3:c.2650_2651delinsAC	XP_011541144.1:p.Thr884=
XM_011542843.2:c.2815_2816delinsAC	XP_011541145.1:p.Thr939=
XM_011542844.3:c.1771_1772delinsAC	XP_011541146.1:p.Thr591=
XM_011542845.2:c.1507_1508delinsAC	XP_011541147.1:p.Thr503=
XM_017017789.2:c.2815_2816delinsAC	XP_016873278.1:p.Thr939=
XM_017017790.2:c.2815_2816delinsAC	XP_016873279.1:p.Thr939=
XM_017017791.1:c.2815_2816delinsAC	XP_016873280.1:p.Thr939=
XM_017017792.2:c.2815_2816delinsAC	XP_016873281.1:p.Thr939=
XR_002957150.1:n.3548_3549delinsAC
NM_001351834.2:c.2815_2816delinsAC	NP_001338763.1:p.Thr939=
NM_000051.4:c.2815_2816delinsAC MANE Select	NP_000042.3:p.Thr939=