Linked Data
ClinVar Variation Id:
127447
ClinVar RCV Id:
RCV000115253
RCV000206201
RCV000212074
RCV000515371
RCV001270954
RCV001253391
RCV003319320
RCV002463639
dbSNP Id:
rs587779866
ExAC:
11:108202604 A / C
gnomAD v2:
11-108202604-A-C
gnomAD v3:
11-108331877-A-C
gnomAD v4:
11-108331877-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108331877A>C , CM000673.2:g.108331877A>C | GRCh38 |
| NC_000011.9:g.108202604A>C , CM000673.1:g.108202604A>C | GRCh37 |
| NC_000011.8:g.107707814A>C | NCBI36 |
| NG_009830.1:g.114046A>C , LRG_135:g.114046A>C | |
| NG_054724.1:g.142956T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.7630-2A>C (ATM) | ENSP00000388058.2:n.7630-2A>C | |
| ENST00000713593.1:c.*7101-2A>C (ATM) | ENSP00000518889.1:n.*7101-2A>C | |
| ENST00000278616.9:c.7630-2A>C (ATM) | ENSP00000278616.4:n.7630-2A>C | |
| ENST00000525056.2:n.2049-2A>C (ATM) | ||
| ENST00000525537.3:n.587-2A>C (ATM) | ||
| ENST00000638786.2:n.467-2A>C (ATM) | ||
| ENST00000682286.1:n.2387-2A>C (ATM) | ||
| ENST00000682302.1:n.2048-2A>C (ATM) | ||
| ENST00000683174.1:n.9114-2A>C (ATM) | ||
| ENST00000683524.1:n.2854-2A>C (ATM) | ||
| ENST00000684152.1:n.3343+320A>C (ATM) | ||
| ENST00000684447.1:n.2412A>C (ATM) | ||
| ENST00000527805.6:c.*2694-2A>C (ATM) | ENSP00000435747.2:n.*2694-2A>C | |
| ENST00000675595.1:c.*2765-2A>C (ATM) | ENSP00000502563.1:n.*2765-2A>C | |
| ENST00000675843.1:c.7630-2A>C (ATM) MANE Select | ENSP00000501606.1:n.7630-2A>C | |
| ENST00000278616.8:c.7630-2A>C (ATM) | ENSP00000278616.4:n.7630-2A>C | |
| ENST00000452508.6:c.7630-2A>C (ATM) | ENSP00000388058.2:n.7630-2A>C | |
| ENST00000524755.5:c.300-310T>G (C11orf65) | ||
| ENST00000524792.5:n.3845-2A>C (ATM) | ||
| ENST00000525729.5:c.641-22806T>G (C11orf65) | ENSP00000433395.1:n.641-22806T>G | |
| ENST00000527531.5:c.*1270-310T>G (C11orf65) | ENSP00000431706.1:n.*1270-310T>G | |
| ENST00000533690.5:n.3034-2A>C (ATM) | ||
| ENST00000615746.4:c.*1270-310T>G (C11orf65) | ENSP00000483537.1:n.*1270-310T>G | |
| NM_000051.3:c.7630-2A>C , LRG_135t1:c.7630-2A>C (ATM) | NP_000042.3:n.7630-2A>C | |
| XM_005271414.3:c.*39-310T>G (C11orf65) | XP_005271471.1:n.*39-310T>G | |
| XM_005271415.3:c.805-310T>G (C11orf65) | XP_005271472.1:n.805-310T>G | |
| XM_005271561.3:c.7630-2A>C (ATM) | XP_005271618.2:n.7630-2A>C | |
| XM_005271562.3:c.7630-2A>C (ATM) | XP_005271619.2:n.7630-2A>C | |
| XM_006718843.2:c.7630-2A>C (ATM) | XP_006718906.1:n.7630-2A>C | |
| XM_006718845.1:c.3586-2A>C (ATM) | XP_006718908.1:n.3586-2A>C | |
| XM_011542840.1:c.7630-2A>C (ATM) | XP_011541142.1:n.7630-2A>C | |
| XM_011542841.1:c.7630-2A>C (ATM) | XP_011541143.1:n.7630-2A>C | |
| XM_011542842.1:c.7465-2A>C (ATM) | XP_011541144.1:n.7465-2A>C | |
| XM_011542843.1:c.7630-2A>C (ATM) | XP_011541145.1:n.7630-2A>C | |
| XM_011542844.1:c.6586-2A>C (ATM) | XP_011541146.1:n.6586-2A>C | |
| XM_011542845.1:c.6322-2A>C (ATM) | XP_011541147.1:n.6322-2A>C | |
| XM_011542847.1:c.2701-2A>C (ATM) | XP_011541149.1:n.2701-2A>C | |
| NM_001330368.1:c.641-22806T>G (C11orf65) | NP_001317297.1:n.641-22806T>G | |
| NM_001351110.1:c.*38+3343T>G (C11orf65) | NP_001338039.1:n.*38+3343T>G | |
| NM_001351834.1:c.7630-2A>C (ATM) | NP_001338763.1:n.7630-2A>C | |
| NR_147053.2:n.2375-310T>G (C11orf65) | ||
| XM_005271414.4:c.*39-310T>G (C11orf65) | XP_005271471.1:n.*39-310T>G | |
| XM_005271415.4:c.805-310T>G (C11orf65) | XP_005271472.1:n.805-310T>G | |
| XM_005271562.5:c.7630-2A>C (ATM) | XP_005271619.2:n.7630-2A>C | |
| XM_006718843.4:c.7630-2A>C (ATM) | XP_006718906.1:n.7630-2A>C | |
| XM_006718845.2:c.3586-2A>C (ATM) | XP_006718908.1:n.3586-2A>C | |
| XM_011542840.3:c.7630-2A>C (ATM) | XP_011541142.1:n.7630-2A>C | |
| XM_011542842.3:c.7465-2A>C (ATM) | XP_011541144.1:n.7465-2A>C | |
| XM_011542843.2:c.7630-2A>C (ATM) | XP_011541145.1:n.7630-2A>C | |
| XM_011542844.3:c.6586-2A>C (ATM) | XP_011541146.1:n.6586-2A>C | |
| XM_011542845.2:c.6322-2A>C (ATM) | XP_011541147.1:n.6322-2A>C | |
| XM_017017789.2:c.7630-2A>C (ATM) | XP_016873278.1:n.7630-2A>C | |
| XM_017017790.2:c.7630-2A>C (ATM) | XP_016873279.1:n.7630-2A>C | |
| NM_001330368.2:c.641-22806T>G (C11orf65) | NP_001317297.1:n.641-22806T>G | |
| NM_001351110.2:c.*38+3343T>G (C11orf65) | NP_001338039.1:n.*38+3343T>G | |
| NM_001351834.2:c.7630-2A>C (ATM) | NP_001338763.1:n.7630-2A>C | |
| NM_000051.4:c.7630-2A>C (ATM) MANE Select | NP_000042.3:n.7630-2A>C | |
| NR_147053.3:n.2373-310T>G (C11orf65) |