Canonical Allele Identifier: CA2580083361

Gene: ATM

Linked Data

• ClinVar Variation Id: 2119728
• ClinVar RCV Id: RCV003033240

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108259005_108259016del , CM000673.2:g.108259005_108259016del	GRCh38
NC_000011.9:g.108129732_108129743del , CM000673.1:g.108129732_108129743del	GRCh37
NC_000011.8:g.107634942_107634953del	NCBI36
NG_009830.1:g.41174_41185del , LRG_135:g.41174_41185del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.2396_2407del	ENSP00000388058.2:p.Ala799_Phe803delinsVal
ENST00000713593.1:c.*1867_*1878del	ENSP00000518889.1:n.*1867_*1878del
ENST00000278616.9:c.2396_2407del	ENSP00000278616.4:p.Ala799_Phe803delinsVal
ENST00000682516.1:n.2530_2541del
ENST00000683174.1:n.2546_2557del
ENST00000683605.1:n.1891_1902del
ENST00000684037.1:c.*1331_*1342del	ENSP00000508245.1:n.*1331_*1342del
ENST00000527805.6:c.2396_2407del	ENSP00000435747.2:p.Ala799_Phe803delinsVal
ENST00000675595.1:c.2231_2242del	ENSP00000502563.1:p.Ala744_Phe748delinsVal
ENST00000675843.1:c.2396_2407del MANE Select	ENSP00000501606.1:p.Ala799_Phe803delinsVal
ENST00000278616.8:c.2396_2407del	ENSP00000278616.4:p.Ala799_Phe803delinsVal
ENST00000452508.6:c.2396_2407del	ENSP00000388058.2:p.Ala799_Phe803delinsVal
ENST00000527805.5:c.2396_2407del	ENSP00000435747.1:p.Ala799_Phe803delinsVal
NM_000051.3:c.2396_2407del , LRG_135t1:c.2396_2407del	NP_000042.3:p.Ala799_Phe803delinsVal
XM_005271561.3:c.2396_2407del	XP_005271618.2:p.Ala799_Phe803delinsVal
XM_005271562.3:c.2396_2407del	XP_005271619.2:p.Ala799_Phe803delinsVal
XM_006718843.2:c.2396_2407del	XP_006718906.1:p.Ala799_Phe803delinsVal
XM_011542840.1:c.2396_2407del	XP_011541142.1:p.Ala799_Phe803delinsVal
XM_011542841.1:c.2396_2407del	XP_011541143.1:p.Ala799_Phe803delinsVal
XM_011542842.1:c.2231_2242del	XP_011541144.1:p.Ala744_Phe748delinsVal
XM_011542843.1:c.2396_2407del	XP_011541145.1:p.Ala799_Phe803delinsVal
XM_011542844.1:c.1352_1363del	XP_011541146.1:p.Ala451_Phe455delinsVal
XM_011542845.1:c.1088_1099del	XP_011541147.1:p.Ala363_Phe367delinsVal
XM_011542846.1:c.2396_2407del	XP_011541148.1:p.Ala799_Phe803delinsVal
NM_001351834.1:c.2396_2407del	NP_001338763.1:p.Ala799_Phe803delinsVal
XM_005271562.5:c.2396_2407del	XP_005271619.2:p.Ala799_Phe803delinsVal
XM_006718843.4:c.2396_2407del	XP_006718906.1:p.Ala799_Phe803delinsVal
XM_011542840.3:c.2396_2407del	XP_011541142.1:p.Ala799_Phe803delinsVal
XM_011542842.3:c.2231_2242del	XP_011541144.1:p.Ala744_Phe748delinsVal
XM_011542843.2:c.2396_2407del	XP_011541145.1:p.Ala799_Phe803delinsVal
XM_011542844.3:c.1352_1363del	XP_011541146.1:p.Ala451_Phe455delinsVal
XM_011542845.2:c.1088_1099del	XP_011541147.1:p.Ala363_Phe367delinsVal
XM_017017789.2:c.2396_2407del	XP_016873278.1:p.Ala799_Phe803delinsVal
XM_017017790.2:c.2396_2407del	XP_016873279.1:p.Ala799_Phe803delinsVal
XM_017017791.1:c.2396_2407del	XP_016873280.1:p.Ala799_Phe803delinsVal
XM_017017792.2:c.2396_2407del	XP_016873281.1:p.Ala799_Phe803delinsVal
XR_002957150.1:n.3129_3140del
NM_001351834.2:c.2396_2407del	NP_001338763.1:p.Ala799_Phe803delinsVal
NM_000051.4:c.2396_2407del MANE Select	NP_000042.3:p.Ala799_Phe803delinsVal