Canonical Allele Identifier: CA1998783247

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108267235_108267236delinsGA , CM000673.2:g.108267235_108267236delinsGA	GRCh38
NC_000011.9:g.108137962_108137963delinsGA , CM000673.1:g.108137962_108137963delinsGA	GRCh37
NC_000011.8:g.107643172_107643173delinsGA	NCBI36
NG_009830.1:g.49404_49405delinsGA , LRG_135:g.49404_49405delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.2531_2532delinsGA	ENSP00000388058.2:p.Gly844=
ENST00000713593.1:c.*2002_*2003delinsGA	ENSP00000518889.1:n.*2002_*2003delinsGA
ENST00000278616.9:c.2531_2532delinsGA	ENSP00000278616.4:p.Gly844=
ENST00000682516.1:n.2665_2666delinsGA
ENST00000683174.1:n.2681_2682delinsGA
ENST00000683605.1:n.2026_2027delinsGA
ENST00000684037.1:c.*1466_*1467delinsGA	ENSP00000508245.1:n.*1466_*1467delinsGA
ENST00000527805.6:c.2531_2532delinsGA	ENSP00000435747.2:p.Gly844=
ENST00000675595.1:c.2366_2367delinsGA	ENSP00000502563.1:p.Gly789=
ENST00000675843.1:c.2531_2532delinsGA MANE Select	ENSP00000501606.1:p.Gly844=
ENST00000278616.8:c.2531_2532delinsGA	ENSP00000278616.4:p.Gly844=
ENST00000452508.6:c.2531_2532delinsGA	ENSP00000388058.2:p.Gly844=
ENST00000527805.5:c.2531_2532delinsGA	ENSP00000435747.1:p.Gly844=
NM_000051.3:c.2531_2532delinsGA , LRG_135t1:c.2531_2532delinsGA	NP_000042.3:p.Gly844=
XM_005271561.3:c.2531_2532delinsGA	XP_005271618.2:p.Gly844=
XM_005271562.3:c.2531_2532delinsGA	XP_005271619.2:p.Gly844=
XM_006718843.2:c.2531_2532delinsGA	XP_006718906.1:p.Gly844=
XM_011542840.1:c.2531_2532delinsGA	XP_011541142.1:p.Gly844=
XM_011542841.1:c.2531_2532delinsGA	XP_011541143.1:p.Gly844=
XM_011542842.1:c.2366_2367delinsGA	XP_011541144.1:p.Gly789=
XM_011542843.1:c.2531_2532delinsGA	XP_011541145.1:p.Gly844=
XM_011542844.1:c.1487_1488delinsGA	XP_011541146.1:p.Gly496=
XM_011542845.1:c.1223_1224delinsGA	XP_011541147.1:p.Gly408=
XM_011542846.1:c.2531_2532delinsGA	XP_011541148.1:p.Gly844=
NM_001351834.1:c.2531_2532delinsGA	NP_001338763.1:p.Gly844=
XM_005271562.5:c.2531_2532delinsGA	XP_005271619.2:p.Gly844=
XM_006718843.4:c.2531_2532delinsGA	XP_006718906.1:p.Gly844=
XM_011542840.3:c.2531_2532delinsGA	XP_011541142.1:p.Gly844=
XM_011542842.3:c.2366_2367delinsGA	XP_011541144.1:p.Gly789=
XM_011542843.2:c.2531_2532delinsGA	XP_011541145.1:p.Gly844=
XM_011542844.3:c.1487_1488delinsGA	XP_011541146.1:p.Gly496=
XM_011542845.2:c.1223_1224delinsGA	XP_011541147.1:p.Gly408=
XM_017017789.2:c.2531_2532delinsGA	XP_016873278.1:p.Gly844=
XM_017017790.2:c.2531_2532delinsGA	XP_016873279.1:p.Gly844=
XM_017017791.1:c.2531_2532delinsGA	XP_016873280.1:p.Gly844=
XM_017017792.2:c.2531_2532delinsGA	XP_016873281.1:p.Gly844=
XR_002957150.1:n.3264_3265delinsGA
NM_001351834.2:c.2531_2532delinsGA	NP_001338763.1:p.Gly844=
NM_000051.4:c.2531_2532delinsGA MANE Select	NP_000042.3:p.Gly844=