Canonical Allele Identifier: CA10579230
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Linked Data

ClinVar Variation Id: 230507
dbSNP Id: rs876658603

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108325394del , CM000673.2:g.108325394del GRCh38
NC_000011.9:g.108196121del , CM000673.1:g.108196121del GRCh37
NC_000011.8:g.107701331del NCBI36
NG_009830.1:g.107563del , LRG_135:g.107563del
NG_054724.1:g.149442del

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.6657del (ATM) ENSP00000388058.2:p.Gln2220ArgfsTer15
ENST00000713593.1:c.*6128del (ATM) ENSP00000518889.1:n.*6128del
ENST00000278616.9:c.6657del (ATM) ENSP00000278616.4:p.Gln2220ArgfsTer15
ENST00000525056.2:n.1076del (ATM)
ENST00000682286.1:n.1414del (ATM)
ENST00000682302.1:n.1075del (ATM)
ENST00000683174.1:n.8141del (ATM)
ENST00000683524.1:n.1881del (ATM)
ENST00000684152.1:n.2371del (ATM)
ENST00000527805.6:c.*1721del (ATM) ENSP00000435747.2:n.*1721del
ENST00000675595.1:c.*1792del (ATM) ENSP00000502563.1:n.*1792del
ENST00000675843.1:c.6657del (ATM) MANE Select ENSP00000501606.1:p.Gln2220ArgfsTer15
ENST00000278616.8:c.6657del (ATM) ENSP00000278616.4:p.Gln2220ArgfsTer15
ENST00000452508.6:c.6657del (ATM) ENSP00000388058.2:p.Gln2220ArgfsTer15
ENST00000524792.5:n.2872del (ATM)
ENST00000525729.5:c.641-16320del (C11orf65) ENSP00000433395.1:n.641-16320del
ENST00000533690.5:n.2061del (ATM)
NM_000051.3:c.6657del , LRG_135t1:c.6657del (ATM) NP_000042.3:p.Gln2220ArgfsTer15
XM_005271561.3:c.6657del (ATM) XP_005271618.2:p.Gln2220ArgfsTer15
XM_005271562.3:c.6657del (ATM) XP_005271619.2:p.Gln2220ArgfsTer15
XM_006718843.2:c.6657del (ATM) XP_006718906.1:p.Gln2220ArgfsTer15
XM_006718845.1:c.2613del (ATM) XP_006718908.1:p.Gln872ArgfsTer15
XM_011542840.1:c.6657del (ATM) XP_011541142.1:p.Gln2220ArgfsTer15
XM_011542841.1:c.6657del (ATM) XP_011541143.1:p.Gln2220ArgfsTer15
XM_011542842.1:c.6492del (ATM) XP_011541144.1:p.Gln2165ArgfsTer15
XM_011542843.1:c.6657del (ATM) XP_011541145.1:p.Gln2220ArgfsTer15
XM_011542844.1:c.5613del (ATM) XP_011541146.1:p.Gln1872ArgfsTer15
XM_011542845.1:c.5349del (ATM) XP_011541147.1:p.Gln1784ArgfsTer15
XM_011542847.1:c.1728del (ATM) XP_011541149.1:p.Gln577ArgfsTer15
NM_001330368.1:c.641-16320del (C11orf65) NP_001317297.1:n.641-16320del
NM_001351110.1:c.*38+9829del (C11orf65) NP_001338039.1:n.*38+9829del
NM_001351834.1:c.6657del (ATM) NP_001338763.1:p.Gln2220ArgfsTer15
XM_005271562.5:c.6657del (ATM) XP_005271619.2:p.Gln2220ArgfsTer15
XM_006718843.4:c.6657del (ATM) XP_006718906.1:p.Gln2220ArgfsTer15
XM_006718845.2:c.2613del (ATM) XP_006718908.1:p.Gln872ArgfsTer15
XM_011542840.3:c.6657del (ATM) XP_011541142.1:p.Gln2220ArgfsTer15
XM_011542842.3:c.6492del (ATM) XP_011541144.1:p.Gln2165ArgfsTer15
XM_011542843.2:c.6657del (ATM) XP_011541145.1:p.Gln2220ArgfsTer15
XM_011542844.3:c.5613del (ATM) XP_011541146.1:p.Gln1872ArgfsTer15
XM_011542845.2:c.5349del (ATM) XP_011541147.1:p.Gln1784ArgfsTer15
XM_017017789.2:c.6657del (ATM) XP_016873278.1:p.Gln2220ArgfsTer15
XM_017017790.2:c.6657del (ATM) XP_016873279.1:p.Gln2220ArgfsTer15
NM_001330368.2:c.641-16320del (C11orf65) NP_001317297.1:n.641-16320del
NM_001351110.2:c.*38+9829del (C11orf65) NP_001338039.1:n.*38+9829del
NM_001351834.2:c.6657del (ATM) NP_001338763.1:p.Gln2220ArgfsTer15
NM_000051.4:c.6657del (ATM) MANE Select NP_000042.3:p.Gln2220ArgfsTer15