Canonical Allele Identifier: CA1998771375

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108251825_108251826delinsGT , CM000673.2:g.108251825_108251826delinsGT	GRCh38
NC_000011.9:g.108122552_108122553delinsGT , CM000673.1:g.108122552_108122553delinsGT	GRCh37
NC_000011.8:g.107627762_107627763delinsGT	NCBI36
NG_009830.1:g.33994_33995delinsGT , LRG_135:g.33994_33995delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.1608-12_1608-11delinsGT	ENSP00000388058.2:n.1608-12_1608-11delins...
ENST00000713593.1:c.*1079-12_*1079-11delinsGT	ENSP00000518889.1:n.*1079-12_*1079-11deli...
ENST00000278616.9:c.1608-12_1608-11delinsGT	ENSP00000278616.4:n.1608-12_1608-11delins...
ENST00000682516.1:n.1742-12_1742-11delinsGT
ENST00000683174.1:n.1758-12_1758-11delinsGT
ENST00000683605.1:n.1103-12_1103-11delinsGT
ENST00000684037.1:c.*543-12_*543-11delinsGT	ENSP00000508245.1:n.*543-12_*543-11delins...
ENST00000684061.1:n.1742-12_1742-11delinsGT
ENST00000527805.6:c.1608-12_1608-11delinsGT	ENSP00000435747.2:n.1608-12_1608-11delins...
ENST00000675595.1:c.1443-12_1443-11delinsGT	ENSP00000502563.1:n.1443-12_1443-11delins...
ENST00000675843.1:c.1608-12_1608-11delinsGT MANE Select	ENSP00000501606.1:n.1608-12_1608-11delins...
ENST00000278616.8:c.1608-12_1608-11delinsGT	ENSP00000278616.4:n.1608-12_1608-11delins...
ENST00000452508.6:c.1608-12_1608-11delinsGT	ENSP00000388058.2:n.1608-12_1608-11delins...
ENST00000527805.5:c.1608-12_1608-11delinsGT	ENSP00000435747.1:n.1608-12_1608-11delins...
NM_000051.3:c.1608-12_1608-11delinsGT , LRG_135t1:c.1608-12_1608-11delinsGT	NP_000042.3:n.1608-12_1608-11delinsGT
XM_005271561.3:c.1608-12_1608-11delinsGT	XP_005271618.2:n.1608-12_1608-11delinsGT
XM_005271562.3:c.1608-12_1608-11delinsGT	XP_005271619.2:n.1608-12_1608-11delinsGT
XM_006718843.2:c.1608-12_1608-11delinsGT	XP_006718906.1:n.1608-12_1608-11delinsGT
XM_011542840.1:c.1608-12_1608-11delinsGT	XP_011541142.1:n.1608-12_1608-11delinsGT
XM_011542841.1:c.1608-12_1608-11delinsGT	XP_011541143.1:n.1608-12_1608-11delinsGT
XM_011542842.1:c.1443-12_1443-11delinsGT	XP_011541144.1:n.1443-12_1443-11delinsGT
XM_011542843.1:c.1608-12_1608-11delinsGT	XP_011541145.1:n.1608-12_1608-11delinsGT
XM_011542844.1:c.564-12_564-11delinsGT	XP_011541146.1:n.564-12_564-11delinsGT
XM_011542845.1:c.300-12_300-11delinsGT	XP_011541147.1:n.300-12_300-11delinsGT
XM_011542846.1:c.1608-12_1608-11delinsGT	XP_011541148.1:n.1608-12_1608-11delinsGT
NM_001351834.1:c.1608-12_1608-11delinsGT	NP_001338763.1:n.1608-12_1608-11delinsGT
XM_005271562.5:c.1608-12_1608-11delinsGT	XP_005271619.2:n.1608-12_1608-11delinsGT
XM_006718843.4:c.1608-12_1608-11delinsGT	XP_006718906.1:n.1608-12_1608-11delinsGT
XM_011542840.3:c.1608-12_1608-11delinsGT	XP_011541142.1:n.1608-12_1608-11delinsGT
XM_011542842.3:c.1443-12_1443-11delinsGT	XP_011541144.1:n.1443-12_1443-11delinsGT
XM_011542843.2:c.1608-12_1608-11delinsGT	XP_011541145.1:n.1608-12_1608-11delinsGT
XM_011542844.3:c.564-12_564-11delinsGT	XP_011541146.1:n.564-12_564-11delinsGT
XM_011542845.2:c.300-12_300-11delinsGT	XP_011541147.1:n.300-12_300-11delinsGT
XM_017017789.2:c.1608-12_1608-11delinsGT	XP_016873278.1:n.1608-12_1608-11delinsGT
XM_017017790.2:c.1608-12_1608-11delinsGT	XP_016873279.1:n.1608-12_1608-11delinsGT
XM_017017791.1:c.1608-12_1608-11delinsGT	XP_016873280.1:n.1608-12_1608-11delinsGT
XM_017017792.2:c.1608-12_1608-11delinsGT	XP_016873281.1:n.1608-12_1608-11delinsGT
XR_002957150.1:n.2341-12_2341-11delinsGT
NM_001351834.2:c.1608-12_1608-11delinsGT	NP_001338763.1:n.1608-12_1608-11delinsGT
NM_000051.4:c.1608-12_1608-11delinsGT MANE Select	NP_000042.3:n.1608-12_1608-11delinsGT