Canonical Allele Identifier: CA1998763196

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108243827_108243832delinsATAAAT , CM000673.2:g.108243827_108243832delinsATAAAT	GRCh38
NC_000011.9:g.108114554_108114559delinsATAAAT , CM000673.1:g.108114554_108114559delinsATAAAT	GRCh37
NC_000011.8:g.107619764_107619769delinsATAAAT	NCBI36
NG_009830.1:g.25996_26001delinsATAAAT , LRG_135:g.25996_26001delinsATAAAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.497-126_497-121delinsATAAAT	ENSP00000388058.2:n.497-126_497-121delinsATAAAT
ENST00000713593.1:c.497-148_497-143delinsATAAAT	ENSP00000518889.1:n.497-148_497-143delinsATAAAT
ENST00000278616.9:c.497-126_497-121delinsATAAAT	ENSP00000278616.4:n.497-126_497-121delinsATAAAT
ENST00000682430.1:n.596-126_596-121delinsATAAAT
ENST00000682516.1:n.631-126_631-121delinsATAAAT
ENST00000682956.1:n.631-126_631-121delinsATAAAT
ENST00000683100.1:n.2049_2054delinsATAAAT
ENST00000683174.1:n.647-126_647-121delinsATAAAT
ENST00000684037.1:c.497-126_497-121delinsATAAAT	ENSP00000508245.1:n.497-126_497-121delinsATAAAT
ENST00000684061.1:n.631-126_631-121delinsATAAAT
ENST00000684179.1:n.466-126_466-121delinsATAAAT
ENST00000527805.6:c.497-126_497-121delinsATAAAT	ENSP00000435747.2:n.497-126_497-121delinsATAAAT
ENST00000675595.1:c.332-126_332-121delinsATAAAT	ENSP00000502563.1:n.332-126_332-121delinsATAAAT
ENST00000675843.1:c.497-126_497-121delinsATAAAT MANE Select	ENSP00000501606.1:n.497-126_497-121delinsATAAAT
ENST00000278616.8:c.497-126_497-121delinsATAAAT	ENSP00000278616.4:n.497-126_497-121delinsATAAAT
ENST00000452508.6:c.497-126_497-121delinsATAAAT	ENSP00000388058.2:n.497-126_497-121delinsATAAAT
ENST00000527805.5:c.497-126_497-121delinsATAAAT	ENSP00000435747.1:n.497-126_497-121delinsATAAAT
ENST00000527891.5:c.332-126_332-121delinsATAAAT	ENSP00000433955.1:n.332-126_332-121delinsATAAAT
NM_000051.3:c.497-126_497-121delinsATAAAT , LRG_135t1:c.497-126_497-121delinsATAAAT	NP_000042.3:n.497-126_497-121delinsATAAAT
XM_005271561.3:c.497-126_497-121delinsATAAAT	XP_005271618.2:n.497-126_497-121delinsATAAAT
XM_005271562.3:c.497-126_497-121delinsATAAAT	XP_005271619.2:n.497-126_497-121delinsATAAAT
XM_006718843.2:c.497-126_497-121delinsATAAAT	XP_006718906.1:n.497-126_497-121delinsATAAAT
XM_011542840.1:c.497-126_497-121delinsATAAAT	XP_011541142.1:n.497-126_497-121delinsATAAAT
XM_011542841.1:c.497-126_497-121delinsATAAAT	XP_011541143.1:n.497-126_497-121delinsATAAAT
XM_011542842.1:c.332-126_332-121delinsATAAAT	XP_011541144.1:n.332-126_332-121delinsATAAAT
XM_011542843.1:c.497-126_497-121delinsATAAAT	XP_011541145.1:n.497-126_497-121delinsATAAAT
XM_011542844.1:c.-526-148_-526-143delinsATAAAT	XP_011541146.1:n.-526-148_-526-143delinsATAAAT
XM_011542846.1:c.497-126_497-121delinsATAAAT	XP_011541148.1:n.497-126_497-121delinsATAAAT
NM_001351834.1:c.497-126_497-121delinsATAAAT	NP_001338763.1:n.497-126_497-121delinsATAAAT
XM_005271562.5:c.497-126_497-121delinsATAAAT	XP_005271619.2:n.497-126_497-121delinsATAAAT
XM_006718843.4:c.497-126_497-121delinsATAAAT	XP_006718906.1:n.497-126_497-121delinsATAAAT
XM_011542840.3:c.497-126_497-121delinsATAAAT	XP_011541142.1:n.497-126_497-121delinsATAAAT
XM_011542842.3:c.332-126_332-121delinsATAAAT	XP_011541144.1:n.332-126_332-121delinsATAAAT
XM_011542843.2:c.497-126_497-121delinsATAAAT	XP_011541145.1:n.497-126_497-121delinsATAAAT
XM_011542844.3:c.-526-148_-526-143delinsATAAAT	XP_011541146.1:n.-526-148_-526-143delinsATAAAT
XM_017017789.2:c.497-126_497-121delinsATAAAT	XP_016873278.1:n.497-126_497-121delinsATAAAT
XM_017017790.2:c.497-126_497-121delinsATAAAT	XP_016873279.1:n.497-126_497-121delinsATAAAT
XM_017017791.1:c.497-126_497-121delinsATAAAT	XP_016873280.1:n.497-126_497-121delinsATAAAT
XM_017017792.2:c.497-126_497-121delinsATAAAT	XP_016873281.1:n.497-126_497-121delinsATAAAT
XR_002957150.1:n.1230-126_1230-121delinsATAAAT
NM_001351834.2:c.497-126_497-121delinsATAAAT	NP_001338763.1:n.497-126_497-121delinsATAAAT
NM_000051.4:c.497-126_497-121delinsATAAAT MANE Select	NP_000042.3:n.497-126_497-121delinsATAAAT