Linked Data
ClinVar Variation Id:
383023
dbSNP Id:
rs1057521506
gnomAD v2:
11-108206682-T-G
gnomAD v4:
11-108335955-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108335955T>G , CM000673.2:g.108335955T>G | GRCh38 |
| NC_000011.9:g.108206682T>G , CM000673.1:g.108206682T>G | GRCh37 |
| NC_000011.8:g.107711892T>G | NCBI36 |
| NG_009830.1:g.118124T>G , LRG_135:g.118124T>G | |
| NG_054724.1:g.138878A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.8262T>G (ATM) | ENSP00000388058.2:p.Thr2754= | |
| ENST00000713593.1:c.*7733T>G (ATM) | ENSP00000518889.1:n.*7733T>G | |
| ENST00000278616.9:c.8262T>G (ATM) | ENSP00000278616.4:p.Thr2754= | |
| ENST00000525056.2:n.2681T>G (ATM) | ||
| ENST00000638786.2:n.960T>G (ATM) | ||
| ENST00000682286.1:n.3019T>G (ATM) | ||
| ENST00000682302.1:n.2680T>G (ATM) | ||
| ENST00000683174.1:n.9746T>G (ATM) | ||
| ENST00000683524.1:n.3486T>G (ATM) | ||
| ENST00000684152.1:n.3678T>G (ATM) | ||
| ENST00000684180.1:n.736T>G (ATM) | ||
| ENST00000684447.1:n.4755T>G (ATM) | ||
| ENST00000527805.6:c.*3326T>G (ATM) | ENSP00000435747.2:n.*3326T>G | |
| ENST00000675595.1:c.*3397T>G (ATM) | ENSP00000502563.1:n.*3397T>G | |
| ENST00000675843.1:c.8262T>G (ATM) MANE Select | ENSP00000501606.1:p.Thr2754= | |
| ENST00000278616.8:c.8262T>G (ATM) | ENSP00000278616.4:p.Thr2754= | |
| ENST00000452508.6:c.8262T>G (ATM) | ENSP00000388058.2:p.Thr2754= | |
| ENST00000524755.5:c.227-663A>C (C11orf65) | ||
| ENST00000524792.5:n.4477T>G (ATM) | ||
| ENST00000525056.1:n.459T>G (ATM) | ||
| ENST00000525729.5:c.641-26884A>C (C11orf65) | ENSP00000433395.1:n.641-26884A>C | |
| ENST00000527531.5:c.*1197-663A>C (C11orf65) | ENSP00000431706.1:n.*1197-663A>C | |
| ENST00000533979.5:n.474T>G (ATM) | ||
| ENST00000615746.4:c.*1197-663A>C (C11orf65) | ENSP00000483537.1:n.*1197-663A>C | |
| NM_000051.3:c.8262T>G , LRG_135t1:c.8262T>G (ATM) | NP_000042.3:p.Thr2754= | |
| XM_005271414.3:c.788-663A>C (C11orf65) | XP_005271471.1:n.788-663A>C | |
| XM_005271415.3:c.732-663A>C (C11orf65) | XP_005271472.1:n.732-663A>C | |
| XM_005271561.3:c.8262T>G (ATM) | XP_005271618.2:p.Thr2754= | |
| XM_005271562.3:c.8262T>G (ATM) | XP_005271619.2:p.Thr2754= | |
| XM_006718843.2:c.8262T>G (ATM) | XP_006718906.1:p.Thr2754= | |
| XM_006718845.1:c.4218T>G (ATM) | XP_006718908.1:p.Thr1406= | |
| XM_011542840.1:c.8262T>G (ATM) | XP_011541142.1:p.Thr2754= | |
| XM_011542841.1:c.8262T>G (ATM) | XP_011541143.1:p.Thr2754= | |
| XM_011542842.1:c.8097T>G (ATM) | XP_011541144.1:p.Thr2699= | |
| XM_011542843.1:c.8262T>G (ATM) | XP_011541145.1:p.Thr2754= | |
| XM_011542844.1:c.7218T>G (ATM) | XP_011541146.1:p.Thr2406= | |
| XM_011542845.1:c.6954T>G (ATM) | XP_011541147.1:p.Thr2318= | |
| XM_011542847.1:c.3333T>G (ATM) | XP_011541149.1:p.Thr1111= | |
| NM_001330368.1:c.641-26884A>C (C11orf65) | NP_001317297.1:n.641-26884A>C | |
| NM_001351110.1:c.695-663A>C (C11orf65) | NP_001338039.1:n.695-663A>C | |
| NM_001351834.1:c.8262T>G (ATM) | NP_001338763.1:p.Thr2754= | |
| NR_147053.2:n.2302-663A>C (C11orf65) | ||
| XM_005271414.4:c.788-663A>C (C11orf65) | XP_005271471.1:n.788-663A>C | |
| XM_005271415.4:c.732-663A>C (C11orf65) | XP_005271472.1:n.732-663A>C | |
| XM_005271562.5:c.8262T>G (ATM) | XP_005271619.2:p.Thr2754= | |
| XM_006718843.4:c.8262T>G (ATM) | XP_006718906.1:p.Thr2754= | |
| XM_006718845.2:c.4218T>G (ATM) | XP_006718908.1:p.Thr1406= | |
| XM_011542840.3:c.8262T>G (ATM) | XP_011541142.1:p.Thr2754= | |
| XM_011542842.3:c.8097T>G (ATM) | XP_011541144.1:p.Thr2699= | |
| XM_011542843.2:c.8262T>G (ATM) | XP_011541145.1:p.Thr2754= | |
| XM_011542844.3:c.7218T>G (ATM) | XP_011541146.1:p.Thr2406= | |
| XM_011542845.2:c.6954T>G (ATM) | XP_011541147.1:p.Thr2318= | |
| XM_017017789.2:c.8262T>G (ATM) | XP_016873278.1:p.Thr2754= | |
| XM_017017790.2:c.8262T>G (ATM) | XP_016873279.1:p.Thr2754= | |
| NM_001330368.2:c.641-26884A>C (C11orf65) | NP_001317297.1:n.641-26884A>C | |
| NM_001351110.2:c.695-663A>C (C11orf65) | NP_001338039.1:n.695-663A>C | |
| NM_001351834.2:c.8262T>G (ATM) | NP_001338763.1:p.Thr2754= | |
| NM_000051.4:c.8262T>G (ATM) MANE Select | NP_000042.3:p.Thr2754= | |
| NR_147053.3:n.2300-663A>C (C11orf65) |