Linked Data
ClinVar Variation Id:
921116
ClinVar RCV Id:
RCV001180266
dbSNP Id:
rs2086407468
gnomAD v3:
11-108332786-A-G
gnomAD v4:
11-108332786-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108332786A>G , CM000673.2:g.108332786A>G | GRCh38 |
| NC_000011.9:g.108203513A>G , CM000673.1:g.108203513A>G | GRCh37 |
| NC_000011.8:g.107708723A>G | NCBI36 |
| NG_009830.1:g.114955A>G , LRG_135:g.114955A>G | |
| NG_054724.1:g.142047T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.7813A>G (ATM) | ENSP00000388058.2:p.Ile2605Val | |
| ENST00000713593.1:c.*7284A>G (ATM) | ENSP00000518889.1:n.*7284A>G | |
| ENST00000278616.9:c.7813A>G (ATM) | ENSP00000278616.4:p.Ile2605Val | |
| ENST00000525056.2:n.2232A>G (ATM) | ||
| ENST00000525537.3:n.1494A>G (ATM) | ||
| ENST00000638786.2:n.625+749A>G (ATM) | ||
| ENST00000682286.1:n.2570A>G (ATM) | ||
| ENST00000682302.1:n.2231A>G (ATM) | ||
| ENST00000683174.1:n.9297A>G (ATM) | ||
| ENST00000683524.1:n.3037A>G (ATM) | ||
| ENST00000684152.1:n.3344-1100A>G (ATM) | ||
| ENST00000684180.1:n.287A>G (ATM) | ||
| ENST00000684447.1:n.3321A>G (ATM) | ||
| ENST00000527805.6:c.*2877A>G (ATM) | ENSP00000435747.2:n.*2877A>G | |
| ENST00000675595.1:c.*2948A>G (ATM) | ENSP00000502563.1:n.*2948A>G | |
| ENST00000675843.1:c.7813A>G (ATM) MANE Select | ENSP00000501606.1:p.Ile2605Val | |
| ENST00000278616.8:c.7813A>G (ATM) | ENSP00000278616.4:p.Ile2605Val | |
| ENST00000452508.6:c.7813A>G (ATM) | ENSP00000388058.2:p.Ile2605Val | |
| ENST00000524755.5:c.300-1219T>C (C11orf65) | ||
| ENST00000524792.5:n.4028A>G (ATM) | ||
| ENST00000525056.1:n.10A>G (ATM) | ||
| ENST00000525729.5:c.641-23715T>C (C11orf65) | ENSP00000433395.1:n.641-23715T>C | |
| ENST00000527531.5:c.*1270-1219T>C (C11orf65) | ENSP00000431706.1:n.*1270-1219T>C | |
| ENST00000533690.5:n.3217A>G (ATM) | ||
| ENST00000533979.5:n.25A>G (ATM) | ||
| ENST00000615746.4:c.*1270-1219T>C (C11orf65) | ENSP00000483537.1:n.*1270-1219T>C | |
| NM_000051.3:c.7813A>G , LRG_135t1:c.7813A>G (ATM) | NP_000042.3:p.Ile2605Val | |
| XM_005271414.3:c.*39-1219T>C (C11orf65) | XP_005271471.1:n.*39-1219T>C | |
| XM_005271415.3:c.805-1219T>C (C11orf65) | XP_005271472.1:n.805-1219T>C | |
| XM_005271561.3:c.7813A>G (ATM) | XP_005271618.2:p.Ile2605Val | |
| XM_005271562.3:c.7813A>G (ATM) | XP_005271619.2:p.Ile2605Val | |
| XM_006718843.2:c.7813A>G (ATM) | XP_006718906.1:p.Ile2605Val | |
| XM_006718845.1:c.3769A>G (ATM) | XP_006718908.1:p.Ile1257Val | |
| XM_011542840.1:c.7813A>G (ATM) | XP_011541142.1:p.Ile2605Val | |
| XM_011542841.1:c.7813A>G (ATM) | XP_011541143.1:p.Ile2605Val | |
| XM_011542842.1:c.7648A>G (ATM) | XP_011541144.1:p.Ile2550Val | |
| XM_011542843.1:c.7813A>G (ATM) | XP_011541145.1:p.Ile2605Val | |
| XM_011542844.1:c.6769A>G (ATM) | XP_011541146.1:p.Ile2257Val | |
| XM_011542845.1:c.6505A>G (ATM) | XP_011541147.1:p.Ile2169Val | |
| XM_011542847.1:c.2884A>G (ATM) | XP_011541149.1:p.Ile962Val | |
| NM_001330368.1:c.641-23715T>C (C11orf65) | NP_001317297.1:n.641-23715T>C | |
| NM_001351110.1:c.*38+2434T>C (C11orf65) | NP_001338039.1:n.*38+2434T>C | |
| NM_001351834.1:c.7813A>G (ATM) | NP_001338763.1:p.Ile2605Val | |
| NR_147053.2:n.2375-1219T>C (C11orf65) | ||
| XM_005271414.4:c.*39-1219T>C (C11orf65) | XP_005271471.1:n.*39-1219T>C | |
| XM_005271415.4:c.805-1219T>C (C11orf65) | XP_005271472.1:n.805-1219T>C | |
| XM_005271562.5:c.7813A>G (ATM) | XP_005271619.2:p.Ile2605Val | |
| XM_006718843.4:c.7813A>G (ATM) | XP_006718906.1:p.Ile2605Val | |
| XM_006718845.2:c.3769A>G (ATM) | XP_006718908.1:p.Ile1257Val | |
| XM_011542840.3:c.7813A>G (ATM) | XP_011541142.1:p.Ile2605Val | |
| XM_011542842.3:c.7648A>G (ATM) | XP_011541144.1:p.Ile2550Val | |
| XM_011542843.2:c.7813A>G (ATM) | XP_011541145.1:p.Ile2605Val | |
| XM_011542844.3:c.6769A>G (ATM) | XP_011541146.1:p.Ile2257Val | |
| XM_011542845.2:c.6505A>G (ATM) | XP_011541147.1:p.Ile2169Val | |
| XM_017017789.2:c.7813A>G (ATM) | XP_016873278.1:p.Ile2605Val | |
| XM_017017790.2:c.7813A>G (ATM) | XP_016873279.1:p.Ile2605Val | |
| NM_001330368.2:c.641-23715T>C (C11orf65) | NP_001317297.1:n.641-23715T>C | |
| NM_001351110.2:c.*38+2434T>C (C11orf65) | NP_001338039.1:n.*38+2434T>C | |
| NM_001351834.2:c.7813A>G (ATM) | NP_001338763.1:p.Ile2605Val | |
| NM_000051.4:c.7813A>G (ATM) MANE Select | NP_000042.3:p.Ile2605Val | |
| NR_147053.3:n.2373-1219T>C (C11orf65) |