Canonical Allele Identifier: CA601727121
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Linked Data

dbSNP Id: rs1183120946

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108332789del , CM000673.2:g.108332789del GRCh38
NC_000011.9:g.108203516del , CM000673.1:g.108203516del GRCh37
NC_000011.8:g.107708726del NCBI36
NG_009830.1:g.114958del , LRG_135:g.114958del
NG_054724.1:g.142045del

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.7816del (ATM) ENSP00000388058.2:p.Ile2606TyrfsTer25
ENST00000713593.1:c.*7287del (ATM) ENSP00000518889.1:n.*7287del
ENST00000278616.9:c.7816del (ATM) ENSP00000278616.4:p.Ile2606TyrfsTer25
ENST00000525056.2:n.2235del (ATM)
ENST00000525537.3:n.1497del (ATM)
ENST00000638786.2:n.625+752del (ATM)
ENST00000682286.1:n.2573del (ATM)
ENST00000682302.1:n.2234del (ATM)
ENST00000683174.1:n.9300del (ATM)
ENST00000683524.1:n.3040del (ATM)
ENST00000684152.1:n.3344-1097del (ATM)
ENST00000684180.1:n.290del (ATM)
ENST00000684447.1:n.3324del (ATM)
ENST00000527805.6:c.*2880del (ATM) ENSP00000435747.2:n.*2880del
ENST00000675595.1:c.*2951del (ATM) ENSP00000502563.1:n.*2951del
ENST00000675843.1:c.7816del (ATM) MANE Select ENSP00000501606.1:p.Ile2606TyrfsTer25
ENST00000278616.8:c.7816del (ATM) ENSP00000278616.4:p.Ile2606TyrfsTer25
ENST00000452508.6:c.7816del (ATM) ENSP00000388058.2:p.Ile2606TyrfsTer25
ENST00000524755.5:c.300-1221del (C11orf65)
ENST00000524792.5:n.4031del (ATM)
ENST00000525056.1:n.13del (ATM)
ENST00000525729.5:c.641-23717del (C11orf65) ENSP00000433395.1:n.641-23717del
ENST00000527531.5:c.*1270-1221del (C11orf65) ENSP00000431706.1:n.*1270-1221del
ENST00000533690.5:n.3220del (ATM)
ENST00000533979.5:n.28del (ATM)
ENST00000615746.4:c.*1270-1221del (C11orf65) ENSP00000483537.1:n.*1270-1221del
NM_000051.3:c.7816del , LRG_135t1:c.7816del (ATM) NP_000042.3:p.Ile2606TyrfsTer25
XM_005271414.3:c.*39-1221del (C11orf65) XP_005271471.1:n.*39-1221del
XM_005271415.3:c.805-1221del (C11orf65) XP_005271472.1:n.805-1221del
XM_005271561.3:c.7816del (ATM) XP_005271618.2:p.Ile2606TyrfsTer25
XM_005271562.3:c.7816del (ATM) XP_005271619.2:p.Ile2606TyrfsTer25
XM_006718843.2:c.7816del (ATM) XP_006718906.1:p.Ile2606TyrfsTer25
XM_006718845.1:c.3772del (ATM) XP_006718908.1:p.Ile1258TyrfsTer25
XM_011542840.1:c.7816del (ATM) XP_011541142.1:p.Ile2606TyrfsTer25
XM_011542841.1:c.7816del (ATM) XP_011541143.1:p.Ile2606TyrfsTer25
XM_011542842.1:c.7651del (ATM) XP_011541144.1:p.Ile2551TyrfsTer25
XM_011542843.1:c.7816del (ATM) XP_011541145.1:p.Ile2606TyrfsTer25
XM_011542844.1:c.6772del (ATM) XP_011541146.1:p.Ile2258TyrfsTer25
XM_011542845.1:c.6508del (ATM) XP_011541147.1:p.Ile2170TyrfsTer25
XM_011542847.1:c.2887del (ATM) XP_011541149.1:p.Ile963TyrfsTer25
NM_001330368.1:c.641-23717del (C11orf65) NP_001317297.1:n.641-23717del
NM_001351110.1:c.*38+2432del (C11orf65) NP_001338039.1:n.*38+2432del
NM_001351834.1:c.7816del (ATM) NP_001338763.1:p.Ile2606TyrfsTer25
NR_147053.2:n.2375-1221del (C11orf65)
XM_005271414.4:c.*39-1221del (C11orf65) XP_005271471.1:n.*39-1221del
XM_005271415.4:c.805-1221del (C11orf65) XP_005271472.1:n.805-1221del
XM_005271562.5:c.7816del (ATM) XP_005271619.2:p.Ile2606TyrfsTer25
XM_006718843.4:c.7816del (ATM) XP_006718906.1:p.Ile2606TyrfsTer25
XM_006718845.2:c.3772del (ATM) XP_006718908.1:p.Ile1258TyrfsTer25
XM_011542840.3:c.7816del (ATM) XP_011541142.1:p.Ile2606TyrfsTer25
XM_011542842.3:c.7651del (ATM) XP_011541144.1:p.Ile2551TyrfsTer25
XM_011542843.2:c.7816del (ATM) XP_011541145.1:p.Ile2606TyrfsTer25
XM_011542844.3:c.6772del (ATM) XP_011541146.1:p.Ile2258TyrfsTer25
XM_011542845.2:c.6508del (ATM) XP_011541147.1:p.Ile2170TyrfsTer25
XM_017017789.2:c.7816del (ATM) XP_016873278.1:p.Ile2606TyrfsTer25
XM_017017790.2:c.7816del (ATM) XP_016873279.1:p.Ile2606TyrfsTer25
NM_001330368.2:c.641-23717del (C11orf65) NP_001317297.1:n.641-23717del
NM_001351110.2:c.*38+2432del (C11orf65) NP_001338039.1:n.*38+2432del
NM_001351834.2:c.7816del (ATM) NP_001338763.1:p.Ile2606TyrfsTer25
NM_000051.4:c.7816del (ATM) MANE Select NP_000042.3:p.Ile2606TyrfsTer25
NR_147053.3:n.2373-1221del (C11orf65)