Canonical Allele Identifier: CA1998791723

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108284188_108284189delinsGT , CM000673.2:g.108284188_108284189delinsGT	GRCh38
NC_000011.9:g.108154915_108154916delinsGT , CM000673.1:g.108154915_108154916delinsGT	GRCh37
NC_000011.8:g.107660125_107660126delinsGT	NCBI36
NG_009830.1:g.66357_66358delinsGT , LRG_135:g.66357_66358delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.3747-39_3747-38delinsGT	ENSP00000388058.2:n.3747-39_3747-38delins...
ENST00000713593.1:c.*3218-39_*3218-38delinsGT	ENSP00000518889.1:n.*3218-39_*3218-38deli...
ENST00000278616.9:c.3747-39_3747-38delinsGT	ENSP00000278616.4:n.3747-39_3747-38delins...
ENST00000682289.1:n.94-39_94-38delinsGT
ENST00000683174.1:n.3897-39_3897-38delinsGT
ENST00000527805.6:c.3747-39_3747-38delinsGT	ENSP00000435747.2:n.3747-39_3747-38delins...
ENST00000675595.1:c.3582-39_3582-38delinsGT	ENSP00000502563.1:n.3582-39_3582-38delins...
ENST00000675843.1:c.3747-39_3747-38delinsGT MANE Select	ENSP00000501606.1:n.3747-39_3747-38delins...
ENST00000278616.8:c.3747-39_3747-38delinsGT	ENSP00000278616.4:n.3747-39_3747-38delins...
ENST00000452508.6:c.3747-39_3747-38delinsGT	ENSP00000388058.2:n.3747-39_3747-38delins...
ENST00000527805.5:c.3747-39_3747-38delinsGT	ENSP00000435747.1:n.3747-39_3747-38delins...
NM_000051.3:c.3747-39_3747-38delinsGT , LRG_135t1:c.3747-39_3747-38delinsGT	NP_000042.3:n.3747-39_3747-38delinsGT
XM_005271561.3:c.3747-39_3747-38delinsGT	XP_005271618.2:n.3747-39_3747-38delinsGT
XM_005271562.3:c.3747-39_3747-38delinsGT	XP_005271619.2:n.3747-39_3747-38delinsGT
XM_006718843.2:c.3747-39_3747-38delinsGT	XP_006718906.1:n.3747-39_3747-38delinsGT
XM_011542840.1:c.3747-39_3747-38delinsGT	XP_011541142.1:n.3747-39_3747-38delinsGT
XM_011542841.1:c.3747-39_3747-38delinsGT	XP_011541143.1:n.3747-39_3747-38delinsGT
XM_011542842.1:c.3582-39_3582-38delinsGT	XP_011541144.1:n.3582-39_3582-38delinsGT
XM_011542843.1:c.3747-39_3747-38delinsGT	XP_011541145.1:n.3747-39_3747-38delinsGT
XM_011542844.1:c.2703-39_2703-38delinsGT	XP_011541146.1:n.2703-39_2703-38delinsGT
XM_011542845.1:c.2439-39_2439-38delinsGT	XP_011541147.1:n.2439-39_2439-38delinsGT
XM_011542846.1:c.3747-39_3747-38delinsGT	XP_011541148.1:n.3747-39_3747-38delinsGT
NM_001351834.1:c.3747-39_3747-38delinsGT	NP_001338763.1:n.3747-39_3747-38delinsGT
XM_005271562.5:c.3747-39_3747-38delinsGT	XP_005271619.2:n.3747-39_3747-38delinsGT
XM_006718843.4:c.3747-39_3747-38delinsGT	XP_006718906.1:n.3747-39_3747-38delinsGT
XM_011542840.3:c.3747-39_3747-38delinsGT	XP_011541142.1:n.3747-39_3747-38delinsGT
XM_011542842.3:c.3582-39_3582-38delinsGT	XP_011541144.1:n.3582-39_3582-38delinsGT
XM_011542843.2:c.3747-39_3747-38delinsGT	XP_011541145.1:n.3747-39_3747-38delinsGT
XM_011542844.3:c.2703-39_2703-38delinsGT	XP_011541146.1:n.2703-39_2703-38delinsGT
XM_011542845.2:c.2439-39_2439-38delinsGT	XP_011541147.1:n.2439-39_2439-38delinsGT
XM_017017789.2:c.3747-39_3747-38delinsGT	XP_016873278.1:n.3747-39_3747-38delinsGT
XM_017017790.2:c.3747-39_3747-38delinsGT	XP_016873279.1:n.3747-39_3747-38delinsGT
XM_017017791.1:c.3747-39_3747-38delinsGT	XP_016873280.1:n.3747-39_3747-38delinsGT
XM_017017792.2:c.3747-39_3747-38delinsGT	XP_016873281.1:n.3747-39_3747-38delinsGT
XR_002957150.1:n.4480-39_4480-38delinsGT
NM_001351834.2:c.3747-39_3747-38delinsGT	NP_001338763.1:n.3747-39_3747-38delinsGT
NM_000051.4:c.3747-39_3747-38delinsGT MANE Select	NP_000042.3:n.3747-39_3747-38delinsGT