Canonical Allele Identifier: CA1998772410

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108253908_108253909delinsAT , CM000673.2:g.108253908_108253909delinsAT	GRCh38
NC_000011.9:g.108124635_108124636delinsAT , CM000673.1:g.108124635_108124636delinsAT	GRCh37
NC_000011.8:g.107629845_107629846delinsAT	NCBI36
NG_009830.1:g.36077_36078delinsAT , LRG_135:g.36077_36078delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.1993_1994delinsAT	ENSP00000388058.2:p.Ile665=
ENST00000713593.1:c.*1464_*1465delinsAT	ENSP00000518889.1:n.*1464_*1465delinsAT
ENST00000278616.9:c.1993_1994delinsAT	ENSP00000278616.4:p.Ile665=
ENST00000682516.1:n.2127_2128delinsAT
ENST00000683174.1:n.2143_2144delinsAT
ENST00000683605.1:n.1488_1489delinsAT
ENST00000684037.1:c.*928_*929delinsAT	ENSP00000508245.1:n.*928_*929delinsAT
ENST00000684061.1:n.2127_2128delinsAT
ENST00000527805.6:c.1993_1994delinsAT	ENSP00000435747.2:p.Ile665=
ENST00000675595.1:c.1828_1829delinsAT	ENSP00000502563.1:p.Ile610=
ENST00000675843.1:c.1993_1994delinsAT MANE Select	ENSP00000501606.1:p.Ile665=
ENST00000278616.8:c.1993_1994delinsAT	ENSP00000278616.4:p.Ile665=
ENST00000452508.6:c.1993_1994delinsAT	ENSP00000388058.2:p.Ile665=
ENST00000525012.5:n.170_171delinsAT
ENST00000527805.5:c.1993_1994delinsAT	ENSP00000435747.1:p.Ile665=
ENST00000533526.1:n.146_147delinsAT
NM_000051.3:c.1993_1994delinsAT , LRG_135t1:c.1993_1994delinsAT	NP_000042.3:p.Ile665=
XM_005271561.3:c.1993_1994delinsAT	XP_005271618.2:p.Ile665=
XM_005271562.3:c.1993_1994delinsAT	XP_005271619.2:p.Ile665=
XM_006718843.2:c.1993_1994delinsAT	XP_006718906.1:p.Ile665=
XM_011542840.1:c.1993_1994delinsAT	XP_011541142.1:p.Ile665=
XM_011542841.1:c.1993_1994delinsAT	XP_011541143.1:p.Ile665=
XM_011542842.1:c.1828_1829delinsAT	XP_011541144.1:p.Ile610=
XM_011542843.1:c.1993_1994delinsAT	XP_011541145.1:p.Ile665=
XM_011542844.1:c.949_950delinsAT	XP_011541146.1:p.Ile317=
XM_011542845.1:c.685_686delinsAT	XP_011541147.1:p.Ile229=
XM_011542846.1:c.1993_1994delinsAT	XP_011541148.1:p.Ile665=
NM_001351834.1:c.1993_1994delinsAT	NP_001338763.1:p.Ile665=
XM_005271562.5:c.1993_1994delinsAT	XP_005271619.2:p.Ile665=
XM_006718843.4:c.1993_1994delinsAT	XP_006718906.1:p.Ile665=
XM_011542840.3:c.1993_1994delinsAT	XP_011541142.1:p.Ile665=
XM_011542842.3:c.1828_1829delinsAT	XP_011541144.1:p.Ile610=
XM_011542843.2:c.1993_1994delinsAT	XP_011541145.1:p.Ile665=
XM_011542844.3:c.949_950delinsAT	XP_011541146.1:p.Ile317=
XM_011542845.2:c.685_686delinsAT	XP_011541147.1:p.Ile229=
XM_017017789.2:c.1993_1994delinsAT	XP_016873278.1:p.Ile665=
XM_017017790.2:c.1993_1994delinsAT	XP_016873279.1:p.Ile665=
XM_017017791.1:c.1993_1994delinsAT	XP_016873280.1:p.Ile665=
XM_017017792.2:c.1993_1994delinsAT	XP_016873281.1:p.Ile665=
XR_002957150.1:n.2726_2727delinsAT
NM_001351834.2:c.1993_1994delinsAT	NP_001338763.1:p.Ile665=
NM_000051.4:c.1993_1994delinsAT MANE Select	NP_000042.3:p.Ile665=