Canonical Allele Identifier: CA2574970734

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108253790_108253791insG , CM000673.2:g.108253790_108253791insG	GRCh38
NC_000011.9:g.108124517_108124518insG , CM000673.1:g.108124517_108124518insG	GRCh37
NC_000011.8:g.107629727_107629728insG	NCBI36
NG_009830.1:g.35959_35960insG , LRG_135:g.35959_35960insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.1899-24_1899-23insG	ENSP00000388058.2:n.1899-24_1899-23insG
ENST00000713593.1:c.*1370-24_*1370-23insG	ENSP00000518889.1:n.*1370-24_*1370-23insG
ENST00000278616.9:c.1899-24_1899-23insG	ENSP00000278616.4:n.1899-24_1899-23insG
ENST00000682516.1:n.2033-24_2033-23insG
ENST00000683174.1:n.2049-24_2049-23insG
ENST00000683605.1:n.1394-24_1394-23insG
ENST00000684037.1:c.*834-24_*834-23insG	ENSP00000508245.1:n.*834-24_*834-23insG
ENST00000684061.1:n.2033-24_2033-23insG
ENST00000527805.6:c.1899-24_1899-23insG	ENSP00000435747.2:n.1899-24_1899-23insG
ENST00000675595.1:c.1734-24_1734-23insG	ENSP00000502563.1:n.1734-24_1734-23insG
ENST00000675843.1:c.1899-24_1899-23insG MANE Select	ENSP00000501606.1:n.1899-24_1899-23insG
ENST00000278616.8:c.1899-24_1899-23insG	ENSP00000278616.4:n.1899-24_1899-23insG
ENST00000452508.6:c.1899-24_1899-23insG	ENSP00000388058.2:n.1899-24_1899-23insG
ENST00000525012.5:n.93-41_93-40insG
ENST00000527805.5:c.1899-24_1899-23insG	ENSP00000435747.1:n.1899-24_1899-23insG
ENST00000533526.1:n.93-65_93-64insG
NM_000051.3:c.1899-24_1899-23insG , LRG_135t1:c.1899-24_1899-23insG	NP_000042.3:n.1899-24_1899-23insG
XM_005271561.3:c.1899-24_1899-23insG	XP_005271618.2:n.1899-24_1899-23insG
XM_005271562.3:c.1899-24_1899-23insG	XP_005271619.2:n.1899-24_1899-23insG
XM_006718843.2:c.1899-24_1899-23insG	XP_006718906.1:n.1899-24_1899-23insG
XM_011542840.1:c.1899-24_1899-23insG	XP_011541142.1:n.1899-24_1899-23insG
XM_011542841.1:c.1899-24_1899-23insG	XP_011541143.1:n.1899-24_1899-23insG
XM_011542842.1:c.1734-24_1734-23insG	XP_011541144.1:n.1734-24_1734-23insG
XM_011542843.1:c.1899-24_1899-23insG	XP_011541145.1:n.1899-24_1899-23insG
XM_011542844.1:c.855-24_855-23insG	XP_011541146.1:n.855-24_855-23insG
XM_011542845.1:c.591-24_591-23insG	XP_011541147.1:n.591-24_591-23insG
XM_011542846.1:c.1899-24_1899-23insG	XP_011541148.1:n.1899-24_1899-23insG
NM_001351834.1:c.1899-24_1899-23insG	NP_001338763.1:n.1899-24_1899-23insG
XM_005271562.5:c.1899-24_1899-23insG	XP_005271619.2:n.1899-24_1899-23insG
XM_006718843.4:c.1899-24_1899-23insG	XP_006718906.1:n.1899-24_1899-23insG
XM_011542840.3:c.1899-24_1899-23insG	XP_011541142.1:n.1899-24_1899-23insG
XM_011542842.3:c.1734-24_1734-23insG	XP_011541144.1:n.1734-24_1734-23insG
XM_011542843.2:c.1899-24_1899-23insG	XP_011541145.1:n.1899-24_1899-23insG
XM_011542844.3:c.855-24_855-23insG	XP_011541146.1:n.855-24_855-23insG
XM_011542845.2:c.591-24_591-23insG	XP_011541147.1:n.591-24_591-23insG
XM_017017789.2:c.1899-24_1899-23insG	XP_016873278.1:n.1899-24_1899-23insG
XM_017017790.2:c.1899-24_1899-23insG	XP_016873279.1:n.1899-24_1899-23insG
XM_017017791.1:c.1899-24_1899-23insG	XP_016873280.1:n.1899-24_1899-23insG
XM_017017792.2:c.1899-24_1899-23insG	XP_016873281.1:n.1899-24_1899-23insG
XR_002957150.1:n.2632-24_2632-23insG
NM_001351834.2:c.1899-24_1899-23insG	NP_001338763.1:n.1899-24_1899-23insG
NM_000051.4:c.1899-24_1899-23insG MANE Select	NP_000042.3:n.1899-24_1899-23insG