Canonical Allele Identifier: CA2825001761

Gene: ATM

Linked Data

• ClinVar Variation Id: 3148576
• ClinVar RCV Id: RCV004442470

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108247057_108247058del , CM000673.2:g.108247057_108247058del	GRCh38
NC_000011.9:g.108117784_108117785del , CM000673.1:g.108117784_108117785del	GRCh37
NC_000011.8:g.107622994_107622995del	NCBI36
NG_009830.1:g.29226_29227del , LRG_135:g.29226_29227del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.995_996del	ENSP00000388058.2:p.Tyr332PhefsTer6
ENST00000713593.1:c.*466_*467del	ENSP00000518889.1:n.*466_*467del
ENST00000278616.9:c.995_996del	ENSP00000278616.4:p.Tyr332PhefsTer6
ENST00000682516.1:n.1129_1130del
ENST00000682956.1:n.1129_1130del
ENST00000683100.1:n.3342_3343del
ENST00000683174.1:n.1145_1146del
ENST00000683605.1:n.490_491del
ENST00000684037.1:c.995_996del	ENSP00000508245.1:p.Tyr332PhefsTer6
ENST00000684061.1:n.1129_1130del
ENST00000684179.1:n.964_965del
ENST00000527805.6:c.995_996del	ENSP00000435747.2:p.Tyr332PhefsTer6
ENST00000675595.1:c.830_831del	ENSP00000502563.1:p.Tyr277PhefsTer6
ENST00000675843.1:c.995_996del MANE Select	ENSP00000501606.1:p.Tyr332PhefsTer6
ENST00000278616.8:c.995_996del	ENSP00000278616.4:p.Tyr332PhefsTer6
ENST00000452508.6:c.995_996del	ENSP00000388058.2:p.Tyr332PhefsTer6
ENST00000527805.5:c.995_996del	ENSP00000435747.1:p.Tyr332PhefsTer6
NM_000051.3:c.995_996del , LRG_135t1:c.995_996del	NP_000042.3:p.Tyr332PhefsTer6
XM_005271561.3:c.995_996del	XP_005271618.2:p.Tyr332PhefsTer6
XM_005271562.3:c.995_996del	XP_005271619.2:p.Tyr332PhefsTer6
XM_006718843.2:c.995_996del	XP_006718906.1:p.Tyr332PhefsTer6
XM_011542840.1:c.995_996del	XP_011541142.1:p.Tyr332PhefsTer6
XM_011542841.1:c.995_996del	XP_011541143.1:p.Tyr332PhefsTer6
XM_011542842.1:c.830_831del	XP_011541144.1:p.Tyr277PhefsTer6
XM_011542843.1:c.995_996del	XP_011541145.1:p.Tyr332PhefsTer6
XM_011542844.1:c.-50_-49del	XP_011541146.1:n.-50_-49del
XM_011542845.1:c.-144_-143del	XP_011541147.1:n.-144_-143del
XM_011542846.1:c.995_996del	XP_011541148.1:p.Tyr332PhefsTer6
NM_001351834.1:c.995_996del	NP_001338763.1:p.Tyr332PhefsTer6
XM_005271562.5:c.995_996del	XP_005271619.2:p.Tyr332PhefsTer6
XM_006718843.4:c.995_996del	XP_006718906.1:p.Tyr332PhefsTer6
XM_011542840.3:c.995_996del	XP_011541142.1:p.Tyr332PhefsTer6
XM_011542842.3:c.830_831del	XP_011541144.1:p.Tyr277PhefsTer6
XM_011542843.2:c.995_996del	XP_011541145.1:p.Tyr332PhefsTer6
XM_011542844.3:c.-50_-49del	XP_011541146.1:n.-50_-49del
XM_011542845.2:c.-144_-143del	XP_011541147.1:n.-144_-143del
XM_017017789.2:c.995_996del	XP_016873278.1:p.Tyr332PhefsTer6
XM_017017790.2:c.995_996del	XP_016873279.1:p.Tyr332PhefsTer6
XM_017017791.1:c.995_996del	XP_016873280.1:p.Tyr332PhefsTer6
XM_017017792.2:c.995_996del	XP_016873281.1:p.Tyr332PhefsTer6
XR_002957150.1:n.1728_1729del
NM_001351834.2:c.995_996del	NP_001338763.1:p.Tyr332PhefsTer6
NM_000051.4:c.995_996del MANE Select	NP_000042.3:p.Tyr332PhefsTer6