Canonical Allele Identifier: CA1998803616

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108307827_108307828delinsAT , CM000673.2:g.108307827_108307828delinsAT	GRCh38
NC_000011.9:g.108178554_108178555delinsAT , CM000673.1:g.108178554_108178555delinsAT	GRCh37
NC_000011.8:g.107683764_107683765delinsAT	NCBI36
NG_009830.1:g.89996_89997delinsAT , LRG_135:g.89996_89997delinsAT
NG_054724.1:g.167005_167006delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5675-70_5675-69delinsAT	ENSP00000388058.2:n.5675-70_5675-69delinsAT
ENST00000713593.1:c.*5146-70_*5146-69delinsAT	ENSP00000518889.1:n.*5146-70_*5146-69delinsAT
ENST00000278616.9:c.5675-70_5675-69delinsAT	ENSP00000278616.4:n.5675-70_5675-69delinsAT
ENST00000525056.2:n.24_25delinsAT
ENST00000682286.1:n.432-70_432-69delinsAT
ENST00000682302.1:n.23_24delinsAT
ENST00000683174.1:n.7159-70_7159-69delinsAT
ENST00000683524.1:n.899-70_899-69delinsAT
ENST00000684152.1:n.1389-70_1389-69delinsAT
ENST00000527805.6:c.*739-70_*739-69delinsAT	ENSP00000435747.2:n.*739-70_*739-69delinsAT
ENST00000675595.1:c.*739-70_*739-69delinsAT	ENSP00000502563.1:n.*739-70_*739-69delinsAT
ENST00000675843.1:c.5675-70_5675-69delinsAT MANE Select	ENSP00000501606.1:n.5675-70_5675-69delinsAT
ENST00000278616.8:c.5675-70_5675-69delinsAT	ENSP00000278616.4:n.5675-70_5675-69delinsAT
ENST00000452508.6:c.5675-70_5675-69delinsAT	ENSP00000388058.2:n.5675-70_5675-69delinsAT
ENST00000524792.5:n.1890-70_1890-69delinsAT
ENST00000529588.5:c.187-2333_187-2332delinsAT
ENST00000533690.5:n.1079-70_1079-69delinsAT
NM_000051.3:c.5675-70_5675-69delinsAT , LRG_135t1:c.5675-70_5675-69delinsAT	NP_000042.3:n.5675-70_5675-69delinsAT
XM_005271561.3:c.5675-70_5675-69delinsAT	XP_005271618.2:n.5675-70_5675-69delinsAT
XM_005271562.3:c.5675-70_5675-69delinsAT	XP_005271619.2:n.5675-70_5675-69delinsAT
XM_006718843.2:c.5675-70_5675-69delinsAT	XP_006718906.1:n.5675-70_5675-69delinsAT
XM_006718845.1:c.1631-70_1631-69delinsAT	XP_006718908.1:n.1631-70_1631-69delinsAT
XM_011542840.1:c.5675-70_5675-69delinsAT	XP_011541142.1:n.5675-70_5675-69delinsAT
XM_011542841.1:c.5675-70_5675-69delinsAT	XP_011541143.1:n.5675-70_5675-69delinsAT
XM_011542842.1:c.5510-70_5510-69delinsAT	XP_011541144.1:n.5510-70_5510-69delinsAT
XM_011542843.1:c.5675-70_5675-69delinsAT	XP_011541145.1:n.5675-70_5675-69delinsAT
XM_011542844.1:c.4631-70_4631-69delinsAT	XP_011541146.1:n.4631-70_4631-69delinsAT
XM_011542845.1:c.4367-70_4367-69delinsAT	XP_011541147.1:n.4367-70_4367-69delinsAT
XM_011542847.1:c.746-70_746-69delinsAT	XP_011541149.1:n.746-70_746-69delinsAT
NM_001351834.1:c.5675-70_5675-69delinsAT	NP_001338763.1:n.5675-70_5675-69delinsAT
XM_005271562.5:c.5675-70_5675-69delinsAT	XP_005271619.2:n.5675-70_5675-69delinsAT
XM_006718843.4:c.5675-70_5675-69delinsAT	XP_006718906.1:n.5675-70_5675-69delinsAT
XM_006718845.2:c.1631-70_1631-69delinsAT	XP_006718908.1:n.1631-70_1631-69delinsAT
XM_011542840.3:c.5675-70_5675-69delinsAT	XP_011541142.1:n.5675-70_5675-69delinsAT
XM_011542842.3:c.5510-70_5510-69delinsAT	XP_011541144.1:n.5510-70_5510-69delinsAT
XM_011542843.2:c.5675-70_5675-69delinsAT	XP_011541145.1:n.5675-70_5675-69delinsAT
XM_011542844.3:c.4631-70_4631-69delinsAT	XP_011541146.1:n.4631-70_4631-69delinsAT
XM_011542845.2:c.4367-70_4367-69delinsAT	XP_011541147.1:n.4367-70_4367-69delinsAT
XM_017017789.2:c.5675-70_5675-69delinsAT	XP_016873278.1:n.5675-70_5675-69delinsAT
XM_017017790.2:c.5675-70_5675-69delinsAT	XP_016873279.1:n.5675-70_5675-69delinsAT
XM_017017791.1:c.5675-70_5675-69delinsAT	XP_016873280.1:n.5675-70_5675-69delinsAT
XR_002957150.1:n.6275-70_6275-69delinsAT
NM_001351834.2:c.5675-70_5675-69delinsAT	NP_001338763.1:n.5675-70_5675-69delinsAT
NM_000051.4:c.5675-70_5675-69delinsAT MANE Select	NP_000042.3:n.5675-70_5675-69delinsAT