Canonical Allele Identifier: CA1998769467

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108240429_108240431delinsTTC , CM000673.2:g.108240429_108240431delinsTTC	GRCh38
NC_000011.9:g.108111156_108111158delinsTTC , CM000673.1:g.108111156_108111158delinsTTC	GRCh37
NC_000011.8:g.107616366_107616368delinsTTC	NCBI36
NG_009830.1:g.22598_22600delinsTTC , LRG_135:g.22598_22600delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.497-3524_497-3522delinsTTC	ENSP00000388058.2:n.497-3524_497-3522delinsTTC
ENST00000713593.1:c.497-3546_497-3544delinsTTC	ENSP00000518889.1:n.497-3546_497-3544delinsTTC
ENST00000278616.9:c.497-3524_497-3522delinsTTC	ENSP00000278616.4:n.497-3524_497-3522delinsTTC
ENST00000682430.1:n.596-3524_596-3522delinsTTC
ENST00000682516.1:n.631-3524_631-3522delinsTTC
ENST00000682956.1:n.631-3524_631-3522delinsTTC
ENST00000683174.1:n.647-3524_647-3522delinsTTC
ENST00000684037.1:c.497-3524_497-3522delinsTTC	ENSP00000508245.1:n.497-3524_497-3522delinsTTC
ENST00000684061.1:n.631-3524_631-3522delinsTTC
ENST00000684179.1:n.466-3524_466-3522delinsTTC
ENST00000527805.6:c.497-3524_497-3522delinsTTC	ENSP00000435747.2:n.497-3524_497-3522delinsTTC
ENST00000675595.1:c.332-3524_332-3522delinsTTC	ENSP00000502563.1:n.332-3524_332-3522delinsTTC
ENST00000675843.1:c.497-3524_497-3522delinsTTC MANE Select	ENSP00000501606.1:n.497-3524_497-3522delinsTTC
ENST00000278616.8:c.497-3524_497-3522delinsTTC	ENSP00000278616.4:n.497-3524_497-3522delinsTTC
ENST00000452508.6:c.497-3524_497-3522delinsTTC	ENSP00000388058.2:n.497-3524_497-3522delinsTTC
ENST00000527805.5:c.497-3524_497-3522delinsTTC	ENSP00000435747.1:n.497-3524_497-3522delinsTTC
ENST00000527891.5:c.332-3524_332-3522delinsTTC	ENSP00000433955.1:n.332-3524_332-3522delinsTTC
NM_000051.3:c.497-3524_497-3522delinsTTC , LRG_135t1:c.497-3524_497-3522delinsTTC	NP_000042.3:n.497-3524_497-3522delinsTTC
XM_005271561.3:c.497-3524_497-3522delinsTTC	XP_005271618.2:n.497-3524_497-3522delinsTTC
XM_005271562.3:c.497-3524_497-3522delinsTTC	XP_005271619.2:n.497-3524_497-3522delinsTTC
XM_006718843.2:c.497-3524_497-3522delinsTTC	XP_006718906.1:n.497-3524_497-3522delinsTTC
XM_011542840.1:c.497-3524_497-3522delinsTTC	XP_011541142.1:n.497-3524_497-3522delinsTTC
XM_011542841.1:c.497-3524_497-3522delinsTTC	XP_011541143.1:n.497-3524_497-3522delinsTTC
XM_011542842.1:c.332-3524_332-3522delinsTTC	XP_011541144.1:n.332-3524_332-3522delinsTTC
XM_011542843.1:c.497-3524_497-3522delinsTTC	XP_011541145.1:n.497-3524_497-3522delinsTTC
XM_011542844.1:c.-526-3546_-526-3544delinsTTC	XP_011541146.1:n.-526-3546_-526-3544delinsTTC
XM_011542846.1:c.497-3524_497-3522delinsTTC	XP_011541148.1:n.497-3524_497-3522delinsTTC
NM_001351834.1:c.497-3524_497-3522delinsTTC	NP_001338763.1:n.497-3524_497-3522delinsTTC
XM_005271562.5:c.497-3524_497-3522delinsTTC	XP_005271619.2:n.497-3524_497-3522delinsTTC
XM_006718843.4:c.497-3524_497-3522delinsTTC	XP_006718906.1:n.497-3524_497-3522delinsTTC
XM_011542840.3:c.497-3524_497-3522delinsTTC	XP_011541142.1:n.497-3524_497-3522delinsTTC
XM_011542842.3:c.332-3524_332-3522delinsTTC	XP_011541144.1:n.332-3524_332-3522delinsTTC
XM_011542843.2:c.497-3524_497-3522delinsTTC	XP_011541145.1:n.497-3524_497-3522delinsTTC
XM_011542844.3:c.-526-3546_-526-3544delinsTTC	XP_011541146.1:n.-526-3546_-526-3544delinsTTC
XM_017017789.2:c.497-3524_497-3522delinsTTC	XP_016873278.1:n.497-3524_497-3522delinsTTC
XM_017017790.2:c.497-3524_497-3522delinsTTC	XP_016873279.1:n.497-3524_497-3522delinsTTC
XM_017017791.1:c.497-3524_497-3522delinsTTC	XP_016873280.1:n.497-3524_497-3522delinsTTC
XM_017017792.2:c.497-3524_497-3522delinsTTC	XP_016873281.1:n.497-3524_497-3522delinsTTC
XR_002957150.1:n.1230-3524_1230-3522delinsTTC
NM_001351834.2:c.497-3524_497-3522delinsTTC	NP_001338763.1:n.497-3524_497-3522delinsTTC
NM_000051.4:c.497-3524_497-3522delinsTTC MANE Select	NP_000042.3:n.497-3524_497-3522delinsTTC