Canonical Allele Identifier: CA1998783856

Gene: ATM

Linked Data

• dbSNP Id: rs2081368226

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108268211_108268212del , CM000673.2:g.108268211_108268212del	GRCh38
NC_000011.9:g.108138938_108138939del , CM000673.1:g.108138938_108138939del	GRCh37
NC_000011.8:g.107644148_107644149del	NCBI36
NG_009830.1:g.50380_50381del , LRG_135:g.50380_50381del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.2639-199_2639-198del	ENSP00000388058.2:n.2639-199_2639-198del
ENST00000713593.1:c.*2110-199_*2110-198del	ENSP00000518889.1:n.*2110-199_*2110-198del
ENST00000278616.9:c.2639-199_2639-198del	ENSP00000278616.4:n.2639-199_2639-198del
ENST00000682516.1:n.2772+869_2772+870del
ENST00000683174.1:n.2789-199_2789-198del
ENST00000684037.1:c.*1573+869_*1573+870del	ENSP00000508245.1:n.*1573+869_*1573+870del
ENST00000527805.6:c.2639-199_2639-198del	ENSP00000435747.2:n.2639-199_2639-198del
ENST00000675595.1:c.2474-199_2474-198del	ENSP00000502563.1:n.2474-199_2474-198del
ENST00000675843.1:c.2639-199_2639-198del MANE Select	ENSP00000501606.1:n.2639-199_2639-198del
ENST00000278616.8:c.2639-199_2639-198del	ENSP00000278616.4:n.2639-199_2639-198del
ENST00000452508.6:c.2639-199_2639-198del	ENSP00000388058.2:n.2639-199_2639-198del
ENST00000527805.5:c.2639-199_2639-198del	ENSP00000435747.1:n.2639-199_2639-198del
NM_000051.3:c.2639-199_2639-198del , LRG_135t1:c.2639-199_2639-198del	NP_000042.3:n.2639-199_2639-198del
XM_005271561.3:c.2639-199_2639-198del	XP_005271618.2:n.2639-199_2639-198del
XM_005271562.3:c.2639-199_2639-198del	XP_005271619.2:n.2639-199_2639-198del
XM_006718843.2:c.2639-199_2639-198del	XP_006718906.1:n.2639-199_2639-198del
XM_011542840.1:c.2639-199_2639-198del	XP_011541142.1:n.2639-199_2639-198del
XM_011542841.1:c.2639-199_2639-198del	XP_011541143.1:n.2639-199_2639-198del
XM_011542842.1:c.2474-199_2474-198del	XP_011541144.1:n.2474-199_2474-198del
XM_011542843.1:c.2639-199_2639-198del	XP_011541145.1:n.2639-199_2639-198del
XM_011542844.1:c.1595-199_1595-198del	XP_011541146.1:n.1595-199_1595-198del
XM_011542845.1:c.1331-199_1331-198del	XP_011541147.1:n.1331-199_1331-198del
XM_011542846.1:c.2639-199_2639-198del	XP_011541148.1:n.2639-199_2639-198del
NM_001351834.1:c.2639-199_2639-198del	NP_001338763.1:n.2639-199_2639-198del
XM_005271562.5:c.2639-199_2639-198del	XP_005271619.2:n.2639-199_2639-198del
XM_006718843.4:c.2639-199_2639-198del	XP_006718906.1:n.2639-199_2639-198del
XM_011542840.3:c.2639-199_2639-198del	XP_011541142.1:n.2639-199_2639-198del
XM_011542842.3:c.2474-199_2474-198del	XP_011541144.1:n.2474-199_2474-198del
XM_011542843.2:c.2639-199_2639-198del	XP_011541145.1:n.2639-199_2639-198del
XM_011542844.3:c.1595-199_1595-198del	XP_011541146.1:n.1595-199_1595-198del
XM_011542845.2:c.1331-199_1331-198del	XP_011541147.1:n.1331-199_1331-198del
XM_017017789.2:c.2639-199_2639-198del	XP_016873278.1:n.2639-199_2639-198del
XM_017017790.2:c.2639-199_2639-198del	XP_016873279.1:n.2639-199_2639-198del
XM_017017791.1:c.2639-199_2639-198del	XP_016873280.1:n.2639-199_2639-198del
XM_017017792.2:c.2639-199_2639-198del	XP_016873281.1:n.2639-199_2639-198del
XR_002957150.1:n.3372-199_3372-198del
NM_001351834.2:c.2639-199_2639-198del	NP_001338763.1:n.2639-199_2639-198del
NM_000051.4:c.2639-199_2639-198del MANE Select	NP_000042.3:n.2639-199_2639-198del