Canonical Allele Identifier: CA1998785739

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108289780_108289781delinsTG , CM000673.2:g.108289780_108289781delinsTG	GRCh38
NC_000011.9:g.108160507_108160508delinsTG , CM000673.1:g.108160507_108160508delinsTG	GRCh37
NC_000011.8:g.107665717_107665718delinsTG	NCBI36
NG_009830.1:g.71949_71950delinsTG , LRG_135:g.71949_71950delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.4415_4416delinsTG	ENSP00000388058.2:p.Leu1472=
ENST00000713593.1:c.*3886_*3887delinsTG	ENSP00000518889.1:n.*3886_*3887delinsTG
ENST00000278616.9:c.4415_4416delinsTG	ENSP00000278616.4:p.Leu1472=
ENST00000533733.6:n.1678_1679delinsTG
ENST00000683174.1:n.4565_4566delinsTG
ENST00000527805.6:c.4415_4416delinsTG	ENSP00000435747.2:p.Leu1472=
ENST00000675595.1:c.4250_4251delinsTG	ENSP00000502563.1:p.Leu1417=
ENST00000675843.1:c.4415_4416delinsTG MANE Select	ENSP00000501606.1:p.Leu1472=
ENST00000278616.8:c.4415_4416delinsTG	ENSP00000278616.4:p.Leu1472=
ENST00000452508.6:c.4415_4416delinsTG	ENSP00000388058.2:p.Leu1472=
ENST00000524792.5:n.630_631delinsTG
ENST00000531525.2:c.422_423delinsTG	ENSP00000434327.2:p.Leu141=
ENST00000533733.5:n.844_845delinsTG
NM_000051.3:c.4415_4416delinsTG , LRG_135t1:c.4415_4416delinsTG	NP_000042.3:p.Leu1472=
XM_005271561.3:c.4415_4416delinsTG	XP_005271618.2:p.Leu1472=
XM_005271562.3:c.4415_4416delinsTG	XP_005271619.2:p.Leu1472=
XM_006718843.2:c.4415_4416delinsTG	XP_006718906.1:p.Leu1472=
XM_006718845.1:c.371_372delinsTG	XP_006718908.1:p.Leu124=
XM_011542840.1:c.4415_4416delinsTG	XP_011541142.1:p.Leu1472=
XM_011542841.1:c.4415_4416delinsTG	XP_011541143.1:p.Leu1472=
XM_011542842.1:c.4250_4251delinsTG	XP_011541144.1:p.Leu1417=
XM_011542843.1:c.4415_4416delinsTG	XP_011541145.1:p.Leu1472=
XM_011542844.1:c.3371_3372delinsTG	XP_011541146.1:p.Leu1124=
XM_011542845.1:c.3107_3108delinsTG	XP_011541147.1:p.Leu1036=
XM_011542846.1:c.4415_4416delinsTG	XP_011541148.1:p.Leu1472=
NM_001351834.1:c.4415_4416delinsTG	NP_001338763.1:p.Leu1472=
XM_005271562.5:c.4415_4416delinsTG	XP_005271619.2:p.Leu1472=
XM_006718843.4:c.4415_4416delinsTG	XP_006718906.1:p.Leu1472=
XM_006718845.2:c.371_372delinsTG	XP_006718908.1:p.Leu124=
XM_011542840.3:c.4415_4416delinsTG	XP_011541142.1:p.Leu1472=
XM_011542842.3:c.4250_4251delinsTG	XP_011541144.1:p.Leu1417=
XM_011542843.2:c.4415_4416delinsTG	XP_011541145.1:p.Leu1472=
XM_011542844.3:c.3371_3372delinsTG	XP_011541146.1:p.Leu1124=
XM_011542845.2:c.3107_3108delinsTG	XP_011541147.1:p.Leu1036=
XM_017017789.2:c.4415_4416delinsTG	XP_016873278.1:p.Leu1472=
XM_017017790.2:c.4415_4416delinsTG	XP_016873279.1:p.Leu1472=
XM_017017791.1:c.4415_4416delinsTG	XP_016873280.1:p.Leu1472=
XM_017017792.2:c.4415_4416delinsTG	XP_016873281.1:p.Leu1472=
XR_002957150.1:n.5148_5149delinsTG
NM_001351834.2:c.4415_4416delinsTG	NP_001338763.1:p.Leu1472=
NM_000051.4:c.4415_4416delinsTG MANE Select	NP_000042.3:p.Leu1472=