Canonical Allele Identifier: CA2695215393

Gene: ATM

Linked Data

• dbSNP Id: rs2135943038

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108304706del , CM000673.2:g.108304706del	GRCh38
NC_000011.9:g.108175433del , CM000673.1:g.108175433del	GRCh37
NC_000011.8:g.107680643del	NCBI36
NG_009830.1:g.86875del , LRG_135:g.86875del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.5528del	ENSP00000388058.2:p.Pro1843HisfsTer3
ENST00000713593.1:c.*4999del	ENSP00000518889.1:n.*4999del
ENST00000278616.9:c.5528del	ENSP00000278616.4:p.Pro1843HisfsTer3
ENST00000683174.1:n.7012del
ENST00000683524.1:n.752del
ENST00000684152.1:n.1242del
ENST00000527805.6:c.*592del	ENSP00000435747.2:n.*592del
ENST00000675595.1:c.*592del	ENSP00000502563.1:n.*592del
ENST00000675843.1:c.5528del MANE Select	ENSP00000501606.1:p.Pro1843HisfsTer3
ENST00000278616.8:c.5528del	ENSP00000278616.4:p.Pro1843HisfsTer3
ENST00000452508.6:c.5528del	ENSP00000388058.2:p.Pro1843HisfsTer3
ENST00000524792.5:n.1743del
ENST00000529588.5:c.40del
ENST00000533690.5:n.932del
NM_000051.3:c.5528del , LRG_135t1:c.5528del	NP_000042.3:p.Pro1843HisfsTer3
XM_005271561.3:c.5528del	XP_005271618.2:p.Pro1843HisfsTer3
XM_005271562.3:c.5528del	XP_005271619.2:p.Pro1843HisfsTer3
XM_006718843.2:c.5528del	XP_006718906.1:p.Pro1843HisfsTer3
XM_006718845.1:c.1484del	XP_006718908.1:p.Pro495HisfsTer3
XM_011542840.1:c.5528del	XP_011541142.1:p.Pro1843HisfsTer3
XM_011542841.1:c.5528del	XP_011541143.1:p.Pro1843HisfsTer3
XM_011542842.1:c.5363del	XP_011541144.1:p.Pro1788HisfsTer3
XM_011542843.1:c.5528del	XP_011541145.1:p.Pro1843HisfsTer3
XM_011542844.1:c.4484del	XP_011541146.1:p.Pro1495HisfsTer3
XM_011542845.1:c.4220del	XP_011541147.1:p.Pro1407HisfsTer3
XM_011542847.1:c.599del	XP_011541149.1:p.Pro200HisfsTer3
NM_001351834.1:c.5528del	NP_001338763.1:p.Pro1843HisfsTer3
XM_005271562.5:c.5528del	XP_005271619.2:p.Pro1843HisfsTer3
XM_006718843.4:c.5528del	XP_006718906.1:p.Pro1843HisfsTer3
XM_006718845.2:c.1484del	XP_006718908.1:p.Pro495HisfsTer3
XM_011542840.3:c.5528del	XP_011541142.1:p.Pro1843HisfsTer3
XM_011542842.3:c.5363del	XP_011541144.1:p.Pro1788HisfsTer3
XM_011542843.2:c.5528del	XP_011541145.1:p.Pro1843HisfsTer3
XM_011542844.3:c.4484del	XP_011541146.1:p.Pro1495HisfsTer3
XM_011542845.2:c.4220del	XP_011541147.1:p.Pro1407HisfsTer3
XM_017017789.2:c.5528del	XP_016873278.1:p.Pro1843HisfsTer3
XM_017017790.2:c.5528del	XP_016873279.1:p.Pro1843HisfsTer3
XM_017017791.1:c.5528del	XP_016873280.1:p.Pro1843HisfsTer3
XR_002957150.1:n.6128del
NM_001351834.2:c.5528del	NP_001338763.1:p.Pro1843HisfsTer3
NM_000051.4:c.5528del MANE Select	NP_000042.3:p.Pro1843HisfsTer3