Canonical Allele Identifier: CA1998795460

Gene: ATM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108287687_108287689delinsCAG , CM000673.2:g.108287687_108287689delinsCAG	GRCh38
NC_000011.9:g.108158414_108158416delinsCAG , CM000673.1:g.108158414_108158416delinsCAG	GRCh37
NC_000011.8:g.107663624_107663626delinsCAG	NCBI36
NG_009830.1:g.69856_69858delinsCAG , LRG_135:g.69856_69858delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.4081_4083delinsCAG	ENSP00000388058.2:p.Gln1361=
ENST00000713593.1:c.*3552_*3554delinsCAG	ENSP00000518889.1:n.*3552_*3554delinsCAG
ENST00000278616.9:c.4081_4083delinsCAG	ENSP00000278616.4:p.Gln1361=
ENST00000533733.6:n.1344_1346delinsCAG
ENST00000683174.1:n.4231_4233delinsCAG
ENST00000527805.6:c.4081_4083delinsCAG	ENSP00000435747.2:p.Gln1361=
ENST00000675595.1:c.3916_3918delinsCAG	ENSP00000502563.1:p.Gln1306=
ENST00000675843.1:c.4081_4083delinsCAG MANE Select	ENSP00000501606.1:p.Gln1361=
ENST00000278616.8:c.4081_4083delinsCAG	ENSP00000278616.4:p.Gln1361=
ENST00000452508.6:c.4081_4083delinsCAG	ENSP00000388058.2:p.Gln1361=
ENST00000524792.5:n.296_298delinsCAG
ENST00000527805.5:c.4081_4083delinsCAG	ENSP00000435747.1:p.Gln1361=
ENST00000531525.2:c.88_90delinsCAG	ENSP00000434327.2:p.Gln30=
ENST00000533733.5:n.510_512delinsCAG
NM_000051.3:c.4081_4083delinsCAG , LRG_135t1:c.4081_4083delinsCAG	NP_000042.3:p.Gln1361=
XM_005271561.3:c.4081_4083delinsCAG	XP_005271618.2:p.Gln1361=
XM_005271562.3:c.4081_4083delinsCAG	XP_005271619.2:p.Gln1361=
XM_006718843.2:c.4081_4083delinsCAG	XP_006718906.1:p.Gln1361=
XM_006718845.1:c.37_39delinsCAG	XP_006718908.1:p.Gln13=
XM_011542840.1:c.4081_4083delinsCAG	XP_011541142.1:p.Gln1361=
XM_011542841.1:c.4081_4083delinsCAG	XP_011541143.1:p.Gln1361=
XM_011542842.1:c.3916_3918delinsCAG	XP_011541144.1:p.Gln1306=
XM_011542843.1:c.4081_4083delinsCAG	XP_011541145.1:p.Gln1361=
XM_011542844.1:c.3037_3039delinsCAG	XP_011541146.1:p.Gln1013=
XM_011542845.1:c.2773_2775delinsCAG	XP_011541147.1:p.Gln925=
XM_011542846.1:c.4081_4083delinsCAG	XP_011541148.1:p.Gln1361=
NM_001351834.1:c.4081_4083delinsCAG	NP_001338763.1:p.Gln1361=
XM_005271562.5:c.4081_4083delinsCAG	XP_005271619.2:p.Gln1361=
XM_006718843.4:c.4081_4083delinsCAG	XP_006718906.1:p.Gln1361=
XM_006718845.2:c.37_39delinsCAG	XP_006718908.1:p.Gln13=
XM_011542840.3:c.4081_4083delinsCAG	XP_011541142.1:p.Gln1361=
XM_011542842.3:c.3916_3918delinsCAG	XP_011541144.1:p.Gln1306=
XM_011542843.2:c.4081_4083delinsCAG	XP_011541145.1:p.Gln1361=
XM_011542844.3:c.3037_3039delinsCAG	XP_011541146.1:p.Gln1013=
XM_011542845.2:c.2773_2775delinsCAG	XP_011541147.1:p.Gln925=
XM_017017789.2:c.4081_4083delinsCAG	XP_016873278.1:p.Gln1361=
XM_017017790.2:c.4081_4083delinsCAG	XP_016873279.1:p.Gln1361=
XM_017017791.1:c.4081_4083delinsCAG	XP_016873280.1:p.Gln1361=
XM_017017792.2:c.4081_4083delinsCAG	XP_016873281.1:p.Gln1361=
XR_002957150.1:n.4814_4816delinsCAG
NM_001351834.2:c.4081_4083delinsCAG	NP_001338763.1:p.Gln1361=
NM_000051.4:c.4081_4083delinsCAG MANE Select	NP_000042.3:p.Gln1361=