Canonical Allele Identifier: CA1998796059

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108288979_108288980delinsAT , CM000673.2:g.108288979_108288980delinsAT	GRCh38
NC_000011.9:g.108159706_108159707delinsAT , CM000673.1:g.108159706_108159707delinsAT	GRCh37
NC_000011.8:g.107664916_107664917delinsAT	NCBI36
NG_009830.1:g.71148_71149delinsAT , LRG_135:g.71148_71149delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.4112_4113delinsAT	ENSP00000388058.2:p.Asp1371=
ENST00000713593.1:c.*3583_*3584delinsAT	ENSP00000518889.1:n.*3583_*3584delinsAT
ENST00000278616.9:c.4112_4113delinsAT	ENSP00000278616.4:p.Asp1371=
ENST00000533733.6:n.1375_1376delinsAT
ENST00000683174.1:n.4262_4263delinsAT
ENST00000527805.6:c.4112_4113delinsAT	ENSP00000435747.2:p.Asp1371=
ENST00000675595.1:c.3947_3948delinsAT	ENSP00000502563.1:p.Asp1316=
ENST00000675843.1:c.4112_4113delinsAT MANE Select	ENSP00000501606.1:p.Asp1371=
ENST00000278616.8:c.4112_4113delinsAT	ENSP00000278616.4:p.Asp1371=
ENST00000452508.6:c.4112_4113delinsAT	ENSP00000388058.2:p.Asp1371=
ENST00000524792.5:n.327_328delinsAT
ENST00000531525.2:c.119_120delinsAT	ENSP00000434327.2:p.Asp40=
ENST00000533733.5:n.541_542delinsAT
NM_000051.3:c.4112_4113delinsAT , LRG_135t1:c.4112_4113delinsAT	NP_000042.3:p.Asp1371=
XM_005271561.3:c.4112_4113delinsAT	XP_005271618.2:p.Asp1371=
XM_005271562.3:c.4112_4113delinsAT	XP_005271619.2:p.Asp1371=
XM_006718843.2:c.4112_4113delinsAT	XP_006718906.1:p.Asp1371=
XM_006718845.1:c.68_69delinsAT	XP_006718908.1:p.Asp23=
XM_011542840.1:c.4112_4113delinsAT	XP_011541142.1:p.Asp1371=
XM_011542841.1:c.4112_4113delinsAT	XP_011541143.1:p.Asp1371=
XM_011542842.1:c.3947_3948delinsAT	XP_011541144.1:p.Asp1316=
XM_011542843.1:c.4112_4113delinsAT	XP_011541145.1:p.Asp1371=
XM_011542844.1:c.3068_3069delinsAT	XP_011541146.1:p.Asp1023=
XM_011542845.1:c.2804_2805delinsAT	XP_011541147.1:p.Asp935=
XM_011542846.1:c.4112_4113delinsAT	XP_011541148.1:p.Asp1371=
NM_001351834.1:c.4112_4113delinsAT	NP_001338763.1:p.Asp1371=
XM_005271562.5:c.4112_4113delinsAT	XP_005271619.2:p.Asp1371=
XM_006718843.4:c.4112_4113delinsAT	XP_006718906.1:p.Asp1371=
XM_006718845.2:c.68_69delinsAT	XP_006718908.1:p.Asp23=
XM_011542840.3:c.4112_4113delinsAT	XP_011541142.1:p.Asp1371=
XM_011542842.3:c.3947_3948delinsAT	XP_011541144.1:p.Asp1316=
XM_011542843.2:c.4112_4113delinsAT	XP_011541145.1:p.Asp1371=
XM_011542844.3:c.3068_3069delinsAT	XP_011541146.1:p.Asp1023=
XM_011542845.2:c.2804_2805delinsAT	XP_011541147.1:p.Asp935=
XM_017017789.2:c.4112_4113delinsAT	XP_016873278.1:p.Asp1371=
XM_017017790.2:c.4112_4113delinsAT	XP_016873279.1:p.Asp1371=
XM_017017791.1:c.4112_4113delinsAT	XP_016873280.1:p.Asp1371=
XM_017017792.2:c.4112_4113delinsAT	XP_016873281.1:p.Asp1371=
XR_002957150.1:n.4845_4846delinsAT
NM_001351834.2:c.4112_4113delinsAT	NP_001338763.1:p.Asp1371=
NM_000051.4:c.4112_4113delinsAT MANE Select	NP_000042.3:p.Asp1371=