Linked Data
ClinVar Variation Id:
232389
dbSNP Id:
rs876659735
gnomAD v3:
11-108335063-T-G
gnomAD v4:
11-108335063-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108335063T>G , CM000673.2:g.108335063T>G | GRCh38 |
| NC_000011.9:g.108205790T>G , CM000673.1:g.108205790T>G | GRCh37 |
| NC_000011.8:g.107711000T>G | NCBI36 |
| NG_009830.1:g.117232T>G , LRG_135:g.117232T>G | |
| NG_054724.1:g.139770A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.8105T>G (ATM) | ENSP00000388058.2:p.Ile2702Arg | |
| ENST00000713593.1:c.*7576T>G (ATM) | ENSP00000518889.1:n.*7576T>G | |
| ENST00000278616.9:c.8105T>G (ATM) | ENSP00000278616.4:p.Ile2702Arg | |
| ENST00000525056.2:n.2524T>G (ATM) | ||
| ENST00000638786.2:n.803T>G (ATM) | ||
| ENST00000682286.1:n.2862T>G (ATM) | ||
| ENST00000682302.1:n.2523T>G (ATM) | ||
| ENST00000683174.1:n.9589T>G (ATM) | ||
| ENST00000683524.1:n.3329T>G (ATM) | ||
| ENST00000684152.1:n.3521T>G (ATM) | ||
| ENST00000684180.1:n.579T>G (ATM) | ||
| ENST00000684447.1:n.4598T>G (ATM) | ||
| ENST00000527805.6:c.*3169T>G (ATM) | ENSP00000435747.2:n.*3169T>G | |
| ENST00000675595.1:c.*3240T>G (ATM) | ENSP00000502563.1:n.*3240T>G | |
| ENST00000675843.1:c.8105T>G (ATM) MANE Select | ENSP00000501606.1:p.Ile2702Arg | |
| ENST00000278616.8:c.8105T>G (ATM) | ENSP00000278616.4:p.Ile2702Arg | |
| ENST00000452508.6:c.8105T>G (ATM) | ENSP00000388058.2:p.Ile2702Arg | |
| ENST00000524755.5:c.299+157A>C (C11orf65) | ||
| ENST00000524792.5:n.4320T>G (ATM) | ||
| ENST00000525056.1:n.302T>G (ATM) | ||
| ENST00000525729.5:c.641-25992A>C (C11orf65) | ENSP00000433395.1:n.641-25992A>C | |
| ENST00000527531.5:c.*1269+157A>C (C11orf65) | ENSP00000431706.1:n.*1269+157A>C | |
| ENST00000533979.5:n.317T>G (ATM) | ||
| ENST00000615746.4:c.*1269+157A>C (C11orf65) | ENSP00000483537.1:n.*1269+157A>C | |
| NM_000051.3:c.8105T>G , LRG_135t1:c.8105T>G (ATM) | NP_000042.3:p.Ile2702Arg | |
| XM_005271414.3:c.*38+157A>C (C11orf65) | XP_005271471.1:n.*38+157A>C | |
| XM_005271415.3:c.804+157A>C (C11orf65) | XP_005271472.1:n.804+157A>C | |
| XM_005271561.3:c.8105T>G (ATM) | XP_005271618.2:p.Ile2702Arg | |
| XM_005271562.3:c.8105T>G (ATM) | XP_005271619.2:p.Ile2702Arg | |
| XM_006718843.2:c.8105T>G (ATM) | XP_006718906.1:p.Ile2702Arg | |
| XM_006718845.1:c.4061T>G (ATM) | XP_006718908.1:p.Ile1354Arg | |
| XM_011542840.1:c.8105T>G (ATM) | XP_011541142.1:p.Ile2702Arg | |
| XM_011542841.1:c.8105T>G (ATM) | XP_011541143.1:p.Ile2702Arg | |
| XM_011542842.1:c.7940T>G (ATM) | XP_011541144.1:p.Ile2647Arg | |
| XM_011542843.1:c.8105T>G (ATM) | XP_011541145.1:p.Ile2702Arg | |
| XM_011542844.1:c.7061T>G (ATM) | XP_011541146.1:p.Ile2354Arg | |
| XM_011542845.1:c.6797T>G (ATM) | XP_011541147.1:p.Ile2266Arg | |
| XM_011542847.1:c.3176T>G (ATM) | XP_011541149.1:p.Ile1059Arg | |
| NM_001330368.1:c.641-25992A>C (C11orf65) | NP_001317297.1:n.641-25992A>C | |
| NM_001351110.1:c.*38+157A>C (C11orf65) | NP_001338039.1:n.*38+157A>C | |
| NM_001351834.1:c.8105T>G (ATM) | NP_001338763.1:p.Ile2702Arg | |
| NR_147053.2:n.2374+157A>C (C11orf65) | ||
| XM_005271414.4:c.*38+157A>C (C11orf65) | XP_005271471.1:n.*38+157A>C | |
| XM_005271415.4:c.804+157A>C (C11orf65) | XP_005271472.1:n.804+157A>C | |
| XM_005271562.5:c.8105T>G (ATM) | XP_005271619.2:p.Ile2702Arg | |
| XM_006718843.4:c.8105T>G (ATM) | XP_006718906.1:p.Ile2702Arg | |
| XM_006718845.2:c.4061T>G (ATM) | XP_006718908.1:p.Ile1354Arg | |
| XM_011542840.3:c.8105T>G (ATM) | XP_011541142.1:p.Ile2702Arg | |
| XM_011542842.3:c.7940T>G (ATM) | XP_011541144.1:p.Ile2647Arg | |
| XM_011542843.2:c.8105T>G (ATM) | XP_011541145.1:p.Ile2702Arg | |
| XM_011542844.3:c.7061T>G (ATM) | XP_011541146.1:p.Ile2354Arg | |
| XM_011542845.2:c.6797T>G (ATM) | XP_011541147.1:p.Ile2266Arg | |
| XM_017017789.2:c.8105T>G (ATM) | XP_016873278.1:p.Ile2702Arg | |
| XM_017017790.2:c.8105T>G (ATM) | XP_016873279.1:p.Ile2702Arg | |
| NM_001330368.2:c.641-25992A>C (C11orf65) | NP_001317297.1:n.641-25992A>C | |
| NM_001351110.2:c.*38+157A>C (C11orf65) | NP_001338039.1:n.*38+157A>C | |
| NM_001351834.2:c.8105T>G (ATM) | NP_001338763.1:p.Ile2702Arg | |
| NM_000051.4:c.8105T>G (ATM) MANE Select | NP_000042.3:p.Ile2702Arg | |
| NR_147053.3:n.2372+157A>C (C11orf65) |