Linked Data
dbSNP Id:
rs2087882394
gnomAD v3:
11-108343558-CATAAT-C
gnomAD v4:
11-108343558-CATAAT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108343561_108343565del , CM000673.2:g.108343561_108343565del | GRCh38 |
| NC_000011.9:g.108214288_108214292del , CM000673.1:g.108214288_108214292del | GRCh37 |
| NC_000011.8:g.107719498_107719502del | NCBI36 |
| NG_009830.1:g.125730_125734del , LRG_135:g.125730_125734del | |
| NG_054724.1:g.131270_131274del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.8418+190_8418+194del (ATM) | ENSP00000388058.2:n.8418+190_8418+194del | |
| ENST00000713593.1:c.*7889+190_*7889+194del (ATM) | ENSP00000518889.1:n.*7889+190_*7889+194del | |
| ENST00000278616.9:c.8418+190_8418+194del (ATM) | ENSP00000278616.4:n.8418+190_8418+194del | |
| ENST00000638786.2:n.1116+190_1116+194del (ATM) | ||
| ENST00000682286.1:n.3175+190_3175+194del (ATM) | ||
| ENST00000682302.1:n.2836+190_2836+194del (ATM) | ||
| ENST00000683174.1:n.9902+190_9902+194del (ATM) | ||
| ENST00000683524.1:n.3642+190_3642+194del (ATM) | ||
| ENST00000684152.1:n.3834+190_3834+194del (ATM) | ||
| ENST00000684180.1:n.892+190_892+194del (ATM) | ||
| ENST00000684447.1:n.4911+190_4911+194del (ATM) | ||
| ENST00000527805.6:c.*3482+190_*3482+194del (ATM) | ENSP00000435747.2:n.*3482+190_*3482+194del | |
| ENST00000675595.1:c.*3553+190_*3553+194del (ATM) | ENSP00000502563.1:n.*3553+190_*3553+194del | |
| ENST00000675843.1:c.8418+190_8418+194del (ATM) MANE Select | ENSP00000501606.1:n.8418+190_8418+194del | |
| ENST00000278616.8:c.8418+190_8418+194del (ATM) | ENSP00000278616.4:n.8418+190_8418+194del | |
| ENST00000452508.6:c.8418+190_8418+194del (ATM) | ENSP00000388058.2:n.8418+190_8418+194del | |
| ENST00000524755.5:c.227-8271_227-8267del (C11orf65) | ||
| ENST00000524792.5:n.4633+190_4633+194del (ATM) | ||
| ENST00000525729.5:c.641-34492_641-34488del (C11orf65) | ENSP00000433395.1:n.641-34492_641-34488del | |
| ENST00000526725.1:n.272-3199_272-3195del (C11orf65) | ||
| ENST00000527531.5:c.*1197-8271_*1197-8267del (C11orf65) | ENSP00000431706.1:n.*1197-8271_*1197-8267del | |
| ENST00000615746.4:c.*1197-8271_*1197-8267del (C11orf65) | ENSP00000483537.1:n.*1197-8271_*1197-8267del | |
| NM_000051.3:c.8418+190_8418+194del , LRG_135t1:c.8418+190_8418+194del (ATM) | NP_000042.3:n.8418+190_8418+194del | |
| XM_005271414.3:c.788-8271_788-8267del (C11orf65) | XP_005271471.1:n.788-8271_788-8267del | |
| XM_005271415.3:c.732-8271_732-8267del (C11orf65) | XP_005271472.1:n.732-8271_732-8267del | |
| XM_005271561.3:c.8418+190_8418+194del (ATM) | XP_005271618.2:n.8418+190_8418+194del | |
| XM_005271562.3:c.8418+190_8418+194del (ATM) | XP_005271619.2:n.8418+190_8418+194del | |
| XM_006718843.2:c.8418+190_8418+194del (ATM) | XP_006718906.1:n.8418+190_8418+194del | |
| XM_006718845.1:c.4374+190_4374+194del (ATM) | XP_006718908.1:n.4374+190_4374+194del | |
| XM_011542640.1:c.788-3199_788-3195del (C11orf65) | XP_011540942.1:n.788-3199_788-3195del | |
| XM_011542643.1:c.732-3199_732-3195del (C11orf65) | XP_011540945.1:n.732-3199_732-3195del | |
| XM_011542840.1:c.8418+190_8418+194del (ATM) | XP_011541142.1:n.8418+190_8418+194del | |
| XM_011542841.1:c.8418+190_8418+194del (ATM) | XP_011541143.1:n.8418+190_8418+194del | |
| XM_011542842.1:c.8253+190_8253+194del (ATM) | XP_011541144.1:n.8253+190_8253+194del | |
| XM_011542843.1:c.8418+190_8418+194del (ATM) | XP_011541145.1:n.8418+190_8418+194del | |
| XM_011542844.1:c.7374+190_7374+194del (ATM) | XP_011541146.1:n.7374+190_7374+194del | |
| XM_011542845.1:c.7110+190_7110+194del (ATM) | XP_011541147.1:n.7110+190_7110+194del | |
| XM_011542847.1:c.3489+190_3489+194del (ATM) | XP_011541149.1:n.3489+190_3489+194del | |
| NM_001330368.1:c.641-34492_641-34488del (C11orf65) | NP_001317297.1:n.641-34492_641-34488del | |
| NM_001351110.1:c.695-8271_695-8267del (C11orf65) | NP_001338039.1:n.695-8271_695-8267del | |
| NM_001351834.1:c.8418+190_8418+194del (ATM) | NP_001338763.1:n.8418+190_8418+194del | |
| NR_147053.2:n.2302-8271_2302-8267del (C11orf65) | ||
| XM_005271414.4:c.788-8271_788-8267del (C11orf65) | XP_005271471.1:n.788-8271_788-8267del | |
| XM_005271415.4:c.732-8271_732-8267del (C11orf65) | XP_005271472.1:n.732-8271_732-8267del | |
| XM_005271562.5:c.8418+190_8418+194del (ATM) | XP_005271619.2:n.8418+190_8418+194del | |
| XM_006718843.4:c.8418+190_8418+194del (ATM) | XP_006718906.1:n.8418+190_8418+194del | |
| XM_006718845.2:c.4374+190_4374+194del (ATM) | XP_006718908.1:n.4374+190_4374+194del | |
| XM_011542640.2:c.788-3199_788-3195del (C11orf65) | XP_011540942.1:n.788-3199_788-3195del | |
| XM_011542643.2:c.732-3199_732-3195del (C11orf65) | XP_011540945.1:n.732-3199_732-3195del | |
| XM_011542840.3:c.8418+190_8418+194del (ATM) | XP_011541142.1:n.8418+190_8418+194del | |
| XM_011542842.3:c.8253+190_8253+194del (ATM) | XP_011541144.1:n.8253+190_8253+194del | |
| XM_011542843.2:c.8418+190_8418+194del (ATM) | XP_011541145.1:n.8418+190_8418+194del | |
| XM_011542844.3:c.7374+190_7374+194del (ATM) | XP_011541146.1:n.7374+190_7374+194del | |
| XM_011542845.2:c.7110+190_7110+194del (ATM) | XP_011541147.1:n.7110+190_7110+194del | |
| XM_017017247.1:c.904-3199_904-3195del (C11orf65) | XP_016872736.1:n.904-3199_904-3195del | |
| XM_017017789.2:c.8418+190_8418+194del (ATM) | XP_016873278.1:n.8418+190_8418+194del | |
| XM_017017790.2:c.8418+190_8418+194del (ATM) | XP_016873279.1:n.8418+190_8418+194del | |
| NM_001330368.2:c.641-34492_641-34488del (C11orf65) | NP_001317297.1:n.641-34492_641-34488del | |
| NM_001351110.2:c.695-8271_695-8267del (C11orf65) | NP_001338039.1:n.695-8271_695-8267del | |
| NM_001351834.2:c.8418+190_8418+194del (ATM) | NP_001338763.1:n.8418+190_8418+194del | |
| NM_000051.4:c.8418+190_8418+194del (ATM) MANE Select | NP_000042.3:n.8418+190_8418+194del | |
| NR_147053.3:n.2300-8271_2300-8267del (C11orf65) |