Canonical Allele Identifier: CA1139662184
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Linked Data

ClinVar Variation Id: 971065
dbSNP Id: rs2086411154

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108332807del , CM000673.2:g.108332807del GRCh38
NC_000011.9:g.108203534del , CM000673.1:g.108203534del GRCh37
NC_000011.8:g.107708744del NCBI36
NG_009830.1:g.114976del , LRG_135:g.114976del
NG_054724.1:g.142026del

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.7834del (ATM) ENSP00000388058.2:p.Arg2612GlyfsTer19
ENST00000713593.1:c.*7305del (ATM) ENSP00000518889.1:n.*7305del
ENST00000278616.9:c.7834del (ATM) ENSP00000278616.4:p.Arg2612GlyfsTer19
ENST00000525056.2:n.2253del (ATM)
ENST00000525537.3:n.1515del (ATM)
ENST00000638786.2:n.625+770del (ATM)
ENST00000682286.1:n.2591del (ATM)
ENST00000682302.1:n.2252del (ATM)
ENST00000683174.1:n.9318del (ATM)
ENST00000683524.1:n.3058del (ATM)
ENST00000684152.1:n.3344-1079del (ATM)
ENST00000684180.1:n.308del (ATM)
ENST00000684447.1:n.3342del (ATM)
ENST00000527805.6:c.*2898del (ATM) ENSP00000435747.2:n.*2898del
ENST00000675595.1:c.*2969del (ATM) ENSP00000502563.1:n.*2969del
ENST00000675843.1:c.7834del (ATM) MANE Select ENSP00000501606.1:p.Arg2612GlyfsTer19
ENST00000278616.8:c.7834del (ATM) ENSP00000278616.4:p.Arg2612GlyfsTer19
ENST00000452508.6:c.7834del (ATM) ENSP00000388058.2:p.Arg2612GlyfsTer19
ENST00000524755.5:c.300-1240del (C11orf65)
ENST00000524792.5:n.4049del (ATM)
ENST00000525056.1:n.31del (ATM)
ENST00000525729.5:c.641-23736del (C11orf65) ENSP00000433395.1:n.641-23736del
ENST00000527531.5:c.*1270-1240del (C11orf65) ENSP00000431706.1:n.*1270-1240del
ENST00000533690.5:n.3238del (ATM)
ENST00000533979.5:n.46del (ATM)
ENST00000615746.4:c.*1270-1240del (C11orf65) ENSP00000483537.1:n.*1270-1240del
NM_000051.3:c.7834del , LRG_135t1:c.7834del (ATM) NP_000042.3:p.Arg2612GlyfsTer19
XM_005271414.3:c.*39-1240del (C11orf65) XP_005271471.1:n.*39-1240del
XM_005271415.3:c.805-1240del (C11orf65) XP_005271472.1:n.805-1240del
XM_005271561.3:c.7834del (ATM) XP_005271618.2:p.Arg2612GlyfsTer19
XM_005271562.3:c.7834del (ATM) XP_005271619.2:p.Arg2612GlyfsTer19
XM_006718843.2:c.7834del (ATM) XP_006718906.1:p.Arg2612GlyfsTer19
XM_006718845.1:c.3790del (ATM) XP_006718908.1:p.Arg1264GlyfsTer19
XM_011542840.1:c.7834del (ATM) XP_011541142.1:p.Arg2612GlyfsTer19
XM_011542841.1:c.7834del (ATM) XP_011541143.1:p.Arg2612GlyfsTer19
XM_011542842.1:c.7669del (ATM) XP_011541144.1:p.Arg2557GlyfsTer19
XM_011542843.1:c.7834del (ATM) XP_011541145.1:p.Arg2612GlyfsTer19
XM_011542844.1:c.6790del (ATM) XP_011541146.1:p.Arg2264GlyfsTer19
XM_011542845.1:c.6526del (ATM) XP_011541147.1:p.Arg2176GlyfsTer19
XM_011542847.1:c.2905del (ATM) XP_011541149.1:p.Arg969GlyfsTer19
NM_001330368.1:c.641-23736del (C11orf65) NP_001317297.1:n.641-23736del
NM_001351110.1:c.*38+2413del (C11orf65) NP_001338039.1:n.*38+2413del
NM_001351834.1:c.7834del (ATM) NP_001338763.1:p.Arg2612GlyfsTer19
NR_147053.2:n.2375-1240del (C11orf65)
XM_005271414.4:c.*39-1240del (C11orf65) XP_005271471.1:n.*39-1240del
XM_005271415.4:c.805-1240del (C11orf65) XP_005271472.1:n.805-1240del
XM_005271562.5:c.7834del (ATM) XP_005271619.2:p.Arg2612GlyfsTer19
XM_006718843.4:c.7834del (ATM) XP_006718906.1:p.Arg2612GlyfsTer19
XM_006718845.2:c.3790del (ATM) XP_006718908.1:p.Arg1264GlyfsTer19
XM_011542840.3:c.7834del (ATM) XP_011541142.1:p.Arg2612GlyfsTer19
XM_011542842.3:c.7669del (ATM) XP_011541144.1:p.Arg2557GlyfsTer19
XM_011542843.2:c.7834del (ATM) XP_011541145.1:p.Arg2612GlyfsTer19
XM_011542844.3:c.6790del (ATM) XP_011541146.1:p.Arg2264GlyfsTer19
XM_011542845.2:c.6526del (ATM) XP_011541147.1:p.Arg2176GlyfsTer19
XM_017017789.2:c.7834del (ATM) XP_016873278.1:p.Arg2612GlyfsTer19
XM_017017790.2:c.7834del (ATM) XP_016873279.1:p.Arg2612GlyfsTer19
NM_001330368.2:c.641-23736del (C11orf65) NP_001317297.1:n.641-23736del
NM_001351110.2:c.*38+2413del (C11orf65) NP_001338039.1:n.*38+2413del
NM_001351834.2:c.7834del (ATM) NP_001338763.1:p.Arg2612GlyfsTer19
NM_000051.4:c.7834del (ATM) MANE Select NP_000042.3:p.Arg2612GlyfsTer19
NR_147053.3:n.2373-1240del (C11orf65)