Canonical Allele Identifier: CA1998772306

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108253751_108253755delinsAATAC , CM000673.2:g.108253751_108253755delinsAATAC	GRCh38
NC_000011.9:g.108124478_108124482delinsAATAC , CM000673.1:g.108124478_108124482delinsAATAC	GRCh37
NC_000011.8:g.107629688_107629692delinsAATAC	NCBI36
NG_009830.1:g.35920_35924delinsAATAC , LRG_135:g.35920_35924delinsAATAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.1899-63_1899-59delinsAATAC	ENSP00000388058.2:n.1899-63_1899-59delins...
ENST00000713593.1:c.*1370-63_*1370-59delinsAATAC	ENSP00000518889.1:n.*1370-63_*1370-59deli...
ENST00000278616.9:c.1899-63_1899-59delinsAATAC	ENSP00000278616.4:n.1899-63_1899-59delins...
ENST00000682516.1:n.2033-63_2033-59delinsAATAC
ENST00000683174.1:n.2049-63_2049-59delinsAATAC
ENST00000683605.1:n.1394-63_1394-59delinsAATAC
ENST00000684037.1:c.*834-63_*834-59delinsAATAC	ENSP00000508245.1:n.*834-63_*834-59delins...
ENST00000684061.1:n.2033-63_2033-59delinsAATAC
ENST00000527805.6:c.1899-63_1899-59delinsAATAC	ENSP00000435747.2:n.1899-63_1899-59delins...
ENST00000675595.1:c.1734-63_1734-59delinsAATAC	ENSP00000502563.1:n.1734-63_1734-59delins...
ENST00000675843.1:c.1899-63_1899-59delinsAATAC MANE Select	ENSP00000501606.1:n.1899-63_1899-59delins...
ENST00000278616.8:c.1899-63_1899-59delinsAATAC	ENSP00000278616.4:n.1899-63_1899-59delins...
ENST00000452508.6:c.1899-63_1899-59delinsAATAC	ENSP00000388058.2:n.1899-63_1899-59delins...
ENST00000525012.5:n.93-80_93-76delinsAATAC
ENST00000527805.5:c.1899-63_1899-59delinsAATAC	ENSP00000435747.1:n.1899-63_1899-59delins...
ENST00000533526.1:n.93-104_93-100delinsAATAC
NM_000051.3:c.1899-63_1899-59delinsAATAC , LRG_135t1:c.1899-63_1899-59delinsAATAC	NP_000042.3:n.1899-63_1899-59delinsAATAC
XM_005271561.3:c.1899-63_1899-59delinsAATAC	XP_005271618.2:n.1899-63_1899-59delinsAAT...
XM_005271562.3:c.1899-63_1899-59delinsAATAC	XP_005271619.2:n.1899-63_1899-59delinsAAT...
XM_006718843.2:c.1899-63_1899-59delinsAATAC	XP_006718906.1:n.1899-63_1899-59delinsAAT...
XM_011542840.1:c.1899-63_1899-59delinsAATAC	XP_011541142.1:n.1899-63_1899-59delinsAAT...
XM_011542841.1:c.1899-63_1899-59delinsAATAC	XP_011541143.1:n.1899-63_1899-59delinsAAT...
XM_011542842.1:c.1734-63_1734-59delinsAATAC	XP_011541144.1:n.1734-63_1734-59delinsAAT...
XM_011542843.1:c.1899-63_1899-59delinsAATAC	XP_011541145.1:n.1899-63_1899-59delinsAAT...
XM_011542844.1:c.855-63_855-59delinsAATAC	XP_011541146.1:n.855-63_855-59delinsAATAC...
XM_011542845.1:c.591-63_591-59delinsAATAC	XP_011541147.1:n.591-63_591-59delinsAATAC...
XM_011542846.1:c.1899-63_1899-59delinsAATAC	XP_011541148.1:n.1899-63_1899-59delinsAAT...
NM_001351834.1:c.1899-63_1899-59delinsAATAC	NP_001338763.1:n.1899-63_1899-59delinsAAT...
XM_005271562.5:c.1899-63_1899-59delinsAATAC	XP_005271619.2:n.1899-63_1899-59delinsAAT...
XM_006718843.4:c.1899-63_1899-59delinsAATAC	XP_006718906.1:n.1899-63_1899-59delinsAAT...
XM_011542840.3:c.1899-63_1899-59delinsAATAC	XP_011541142.1:n.1899-63_1899-59delinsAAT...
XM_011542842.3:c.1734-63_1734-59delinsAATAC	XP_011541144.1:n.1734-63_1734-59delinsAAT...
XM_011542843.2:c.1899-63_1899-59delinsAATAC	XP_011541145.1:n.1899-63_1899-59delinsAAT...
XM_011542844.3:c.855-63_855-59delinsAATAC	XP_011541146.1:n.855-63_855-59delinsAATAC...
XM_011542845.2:c.591-63_591-59delinsAATAC	XP_011541147.1:n.591-63_591-59delinsAATAC...
XM_017017789.2:c.1899-63_1899-59delinsAATAC	XP_016873278.1:n.1899-63_1899-59delinsAAT...
XM_017017790.2:c.1899-63_1899-59delinsAATAC	XP_016873279.1:n.1899-63_1899-59delinsAAT...
XM_017017791.1:c.1899-63_1899-59delinsAATAC	XP_016873280.1:n.1899-63_1899-59delinsAAT...
XM_017017792.2:c.1899-63_1899-59delinsAATAC	XP_016873281.1:n.1899-63_1899-59delinsAAT...
XR_002957150.1:n.2632-63_2632-59delinsAATAC
NM_001351834.2:c.1899-63_1899-59delinsAATAC	NP_001338763.1:n.1899-63_1899-59delinsAAT...
NM_000051.4:c.1899-63_1899-59delinsAATAC MANE Select	NP_000042.3:n.1899-63_1899-59delinsAATAC