Canonical Allele Identifier: CA1998791085

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108283467_108283469delinsCTG , CM000673.2:g.108283467_108283469delinsCTG	GRCh38
NC_000011.9:g.108154194_108154196delinsCTG , CM000673.1:g.108154194_108154196delinsCTG	GRCh37
NC_000011.8:g.107659404_107659406delinsCTG	NCBI36
NG_009830.1:g.65636_65638delinsCTG , LRG_135:g.65636_65638delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.3746+588_3746+590delinsCTG	ENSP00000388058.2:n.3746+588_3746+590delinsCTG
ENST00000713593.1:c.*3217+588_*3217+590delinsCTG	ENSP00000518889.1:n.*3217+588_*3217+590delinsCTG
ENST00000278616.9:c.3746+588_3746+590delinsCTG	ENSP00000278616.4:n.3746+588_3746+590delinsCTG
ENST00000682289.1:n.93+588_93+590delinsCTG
ENST00000683174.1:n.3896+588_3896+590delinsCTG
ENST00000527805.6:c.3746+588_3746+590delinsCTG	ENSP00000435747.2:n.3746+588_3746+590delinsCTG
ENST00000675595.1:c.3581+588_3581+590delinsCTG	ENSP00000502563.1:n.3581+588_3581+590delinsCTG
ENST00000675843.1:c.3746+588_3746+590delinsCTG MANE Select	ENSP00000501606.1:n.3746+588_3746+590delinsCTG
ENST00000278616.8:c.3746+588_3746+590delinsCTG	ENSP00000278616.4:n.3746+588_3746+590delinsCTG
ENST00000452508.6:c.3746+588_3746+590delinsCTG	ENSP00000388058.2:n.3746+588_3746+590delinsCTG
ENST00000527805.5:c.3746+588_3746+590delinsCTG	ENSP00000435747.1:n.3746+588_3746+590delinsCTG
NM_000051.3:c.3746+588_3746+590delinsCTG , LRG_135t1:c.3746+588_3746+590delinsCTG	NP_000042.3:n.3746+588_3746+590delinsCTG
XM_005271561.3:c.3746+588_3746+590delinsCTG	XP_005271618.2:n.3746+588_3746+590delinsCTG
XM_005271562.3:c.3746+588_3746+590delinsCTG	XP_005271619.2:n.3746+588_3746+590delinsCTG
XM_006718843.2:c.3746+588_3746+590delinsCTG	XP_006718906.1:n.3746+588_3746+590delinsCTG
XM_011542840.1:c.3746+588_3746+590delinsCTG	XP_011541142.1:n.3746+588_3746+590delinsCTG
XM_011542841.1:c.3746+588_3746+590delinsCTG	XP_011541143.1:n.3746+588_3746+590delinsCTG
XM_011542842.1:c.3581+588_3581+590delinsCTG	XP_011541144.1:n.3581+588_3581+590delinsCTG
XM_011542843.1:c.3746+588_3746+590delinsCTG	XP_011541145.1:n.3746+588_3746+590delinsCTG
XM_011542844.1:c.2702+588_2702+590delinsCTG	XP_011541146.1:n.2702+588_2702+590delinsCTG
XM_011542845.1:c.2438+588_2438+590delinsCTG	XP_011541147.1:n.2438+588_2438+590delinsCTG
XM_011542846.1:c.3746+588_3746+590delinsCTG	XP_011541148.1:n.3746+588_3746+590delinsCTG
NM_001351834.1:c.3746+588_3746+590delinsCTG	NP_001338763.1:n.3746+588_3746+590delinsCTG
XM_005271562.5:c.3746+588_3746+590delinsCTG	XP_005271619.2:n.3746+588_3746+590delinsCTG
XM_006718843.4:c.3746+588_3746+590delinsCTG	XP_006718906.1:n.3746+588_3746+590delinsCTG
XM_011542840.3:c.3746+588_3746+590delinsCTG	XP_011541142.1:n.3746+588_3746+590delinsCTG
XM_011542842.3:c.3581+588_3581+590delinsCTG	XP_011541144.1:n.3581+588_3581+590delinsCTG
XM_011542843.2:c.3746+588_3746+590delinsCTG	XP_011541145.1:n.3746+588_3746+590delinsCTG
XM_011542844.3:c.2702+588_2702+590delinsCTG	XP_011541146.1:n.2702+588_2702+590delinsCTG
XM_011542845.2:c.2438+588_2438+590delinsCTG	XP_011541147.1:n.2438+588_2438+590delinsCTG
XM_017017789.2:c.3746+588_3746+590delinsCTG	XP_016873278.1:n.3746+588_3746+590delinsCTG
XM_017017790.2:c.3746+588_3746+590delinsCTG	XP_016873279.1:n.3746+588_3746+590delinsCTG
XM_017017791.1:c.3746+588_3746+590delinsCTG	XP_016873280.1:n.3746+588_3746+590delinsCTG
XM_017017792.2:c.3746+588_3746+590delinsCTG	XP_016873281.1:n.3746+588_3746+590delinsCTG
XR_002957150.1:n.4479+588_4479+590delinsCTG
NM_001351834.2:c.3746+588_3746+590delinsCTG	NP_001338763.1:n.3746+588_3746+590delinsCTG
NM_000051.4:c.3746+588_3746+590delinsCTG MANE Select	NP_000042.3:n.3746+588_3746+590delinsCTG