Canonical Allele Identifier: CA2615845578

Gene: ATM

Linked Data

• gnomAD v4: 11-108246947-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108246947_108246948insT , CM000673.2:g.108246947_108246948insT	GRCh38
NC_000011.9:g.108117674_108117675insT , CM000673.1:g.108117674_108117675insT	GRCh37
NC_000011.8:g.107622884_107622885insT	NCBI36
NG_009830.1:g.29116_29117insT , LRG_135:g.29116_29117insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.902-17_902-16insT	ENSP00000388058.2:n.902-17_902-16insT
ENST00000713593.1:c.*373-17_*373-16insT	ENSP00000518889.1:n.*373-17_*373-16insT
ENST00000278616.9:c.902-17_902-16insT	ENSP00000278616.4:n.902-17_902-16insT
ENST00000682516.1:n.1036-17_1036-16insT
ENST00000682956.1:n.1036-17_1036-16insT
ENST00000683100.1:n.3249-17_3249-16insT
ENST00000683174.1:n.1052-17_1052-16insT
ENST00000683605.1:n.397-17_397-16insT
ENST00000684037.1:c.902-17_902-16insT	ENSP00000508245.1:n.902-17_902-16insT
ENST00000684061.1:n.1036-17_1036-16insT
ENST00000684179.1:n.871-17_871-16insT
ENST00000527805.6:c.902-17_902-16insT	ENSP00000435747.2:n.902-17_902-16insT
ENST00000675595.1:c.737-17_737-16insT	ENSP00000502563.1:n.737-17_737-16insT
ENST00000675843.1:c.902-17_902-16insT MANE Select	ENSP00000501606.1:n.902-17_902-16insT
ENST00000278616.8:c.902-17_902-16insT	ENSP00000278616.4:n.902-17_902-16insT
ENST00000452508.6:c.902-17_902-16insT	ENSP00000388058.2:n.902-17_902-16insT
ENST00000527805.5:c.902-17_902-16insT	ENSP00000435747.1:n.902-17_902-16insT
NM_000051.3:c.902-17_902-16insT , LRG_135t1:c.902-17_902-16insT	NP_000042.3:n.902-17_902-16insT
XM_005271561.3:c.902-17_902-16insT	XP_005271618.2:n.902-17_902-16insT
XM_005271562.3:c.902-17_902-16insT	XP_005271619.2:n.902-17_902-16insT
XM_006718843.2:c.902-17_902-16insT	XP_006718906.1:n.902-17_902-16insT
XM_011542840.1:c.902-17_902-16insT	XP_011541142.1:n.902-17_902-16insT
XM_011542841.1:c.902-17_902-16insT	XP_011541143.1:n.902-17_902-16insT
XM_011542842.1:c.737-17_737-16insT	XP_011541144.1:n.737-17_737-16insT
XM_011542843.1:c.902-17_902-16insT	XP_011541145.1:n.902-17_902-16insT
XM_011542844.1:c.-143-17_-143-16insT	XP_011541146.1:n.-143-17_-143-16insT
XM_011542846.1:c.902-17_902-16insT	XP_011541148.1:n.902-17_902-16insT
NM_001351834.1:c.902-17_902-16insT	NP_001338763.1:n.902-17_902-16insT
XM_005271562.5:c.902-17_902-16insT	XP_005271619.2:n.902-17_902-16insT
XM_006718843.4:c.902-17_902-16insT	XP_006718906.1:n.902-17_902-16insT
XM_011542840.3:c.902-17_902-16insT	XP_011541142.1:n.902-17_902-16insT
XM_011542842.3:c.737-17_737-16insT	XP_011541144.1:n.737-17_737-16insT
XM_011542843.2:c.902-17_902-16insT	XP_011541145.1:n.902-17_902-16insT
XM_011542844.3:c.-143-17_-143-16insT	XP_011541146.1:n.-143-17_-143-16insT
XM_017017789.2:c.902-17_902-16insT	XP_016873278.1:n.902-17_902-16insT
XM_017017790.2:c.902-17_902-16insT	XP_016873279.1:n.902-17_902-16insT
XM_017017791.1:c.902-17_902-16insT	XP_016873280.1:n.902-17_902-16insT
XM_017017792.2:c.902-17_902-16insT	XP_016873281.1:n.902-17_902-16insT
XR_002957150.1:n.1635-17_1635-16insT
NM_001351834.2:c.902-17_902-16insT	NP_001338763.1:n.902-17_902-16insT
NM_000051.4:c.902-17_902-16insT MANE Select	NP_000042.3:n.902-17_902-16insT