Linked Data
ClinVar Variation Id:
420799
dbSNP Id:
rs876658957
gnomAD v4:
11-108335962-G-A
ERepo:
CA16619252/MONDO:0016419/020
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108335962G>A , CM000673.2:g.108335962G>A | GRCh38 |
| NC_000011.9:g.108206689G>A , CM000673.1:g.108206689G>A | GRCh37 |
| NC_000011.8:g.107711899G>A | NCBI36 |
| NG_009830.1:g.118131G>A , LRG_135:g.118131G>A | |
| NG_054724.1:g.138871C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.8268+1G>A (ATM) | ENSP00000388058.2:n.8268+1G>A | |
| ENST00000713593.1:c.*7739+1G>A (ATM) | ENSP00000518889.1:n.*7739+1G>A | |
| ENST00000278616.9:c.8268+1G>A (ATM) | ENSP00000278616.4:n.8268+1G>A | |
| ENST00000525056.2:n.2688G>A (ATM) | ||
| ENST00000638786.2:n.966+1G>A (ATM) | ||
| ENST00000682286.1:n.3025+1G>A (ATM) | ||
| ENST00000682302.1:n.2686+1G>A (ATM) | ||
| ENST00000683174.1:n.9752+1G>A (ATM) | ||
| ENST00000683524.1:n.3492+1G>A (ATM) | ||
| ENST00000684152.1:n.3684+1G>A (ATM) | ||
| ENST00000684180.1:n.742+1G>A (ATM) | ||
| ENST00000684447.1:n.4761+1G>A (ATM) | ||
| ENST00000527805.6:c.*3332+1G>A (ATM) | ENSP00000435747.2:n.*3332+1G>A | |
| ENST00000675595.1:c.*3403+1G>A (ATM) | ENSP00000502563.1:n.*3403+1G>A | |
| ENST00000675843.1:c.8268+1G>A (ATM) MANE Select | ENSP00000501606.1:n.8268+1G>A | |
| ENST00000278616.8:c.8268+1G>A (ATM) | ENSP00000278616.4:n.8268+1G>A | |
| ENST00000452508.6:c.8268+1G>A (ATM) | ENSP00000388058.2:n.8268+1G>A | |
| ENST00000524755.5:c.227-670C>T (C11orf65) | ||
| ENST00000524792.5:n.4483+1G>A (ATM) | ||
| ENST00000525056.1:n.466G>A (ATM) | ||
| ENST00000525729.5:c.641-26891C>T (C11orf65) | ENSP00000433395.1:n.641-26891C>T | |
| ENST00000527531.5:c.*1197-670C>T (C11orf65) | ENSP00000431706.1:n.*1197-670C>T | |
| ENST00000533979.5:n.480+1G>A (ATM) | ||
| ENST00000615746.4:c.*1197-670C>T (C11orf65) | ENSP00000483537.1:n.*1197-670C>T | |
| NM_000051.3:c.8268+1G>A , LRG_135t1:c.8268+1G>A (ATM) | NP_000042.3:n.8268+1G>A | |
| XM_005271414.3:c.788-670C>T (C11orf65) | XP_005271471.1:n.788-670C>T | |
| XM_005271415.3:c.732-670C>T (C11orf65) | XP_005271472.1:n.732-670C>T | |
| XM_005271561.3:c.8268+1G>A (ATM) | XP_005271618.2:n.8268+1G>A | |
| XM_005271562.3:c.8268+1G>A (ATM) | XP_005271619.2:n.8268+1G>A | |
| XM_006718843.2:c.8268+1G>A (ATM) | XP_006718906.1:n.8268+1G>A | |
| XM_006718845.1:c.4224+1G>A (ATM) | XP_006718908.1:n.4224+1G>A | |
| XM_011542840.1:c.8268+1G>A (ATM) | XP_011541142.1:n.8268+1G>A | |
| XM_011542841.1:c.8268+1G>A (ATM) | XP_011541143.1:n.8268+1G>A | |
| XM_011542842.1:c.8103+1G>A (ATM) | XP_011541144.1:n.8103+1G>A | |
| XM_011542843.1:c.8268+1G>A (ATM) | XP_011541145.1:n.8268+1G>A | |
| XM_011542844.1:c.7224+1G>A (ATM) | XP_011541146.1:n.7224+1G>A | |
| XM_011542845.1:c.6960+1G>A (ATM) | XP_011541147.1:n.6960+1G>A | |
| XM_011542847.1:c.3339+1G>A (ATM) | XP_011541149.1:n.3339+1G>A | |
| NM_001330368.1:c.641-26891C>T (C11orf65) | NP_001317297.1:n.641-26891C>T | |
| NM_001351110.1:c.695-670C>T (C11orf65) | NP_001338039.1:n.695-670C>T | |
| NM_001351834.1:c.8268+1G>A (ATM) | NP_001338763.1:n.8268+1G>A | |
| NR_147053.2:n.2302-670C>T (C11orf65) | ||
| XM_005271414.4:c.788-670C>T (C11orf65) | XP_005271471.1:n.788-670C>T | |
| XM_005271415.4:c.732-670C>T (C11orf65) | XP_005271472.1:n.732-670C>T | |
| XM_005271562.5:c.8268+1G>A (ATM) | XP_005271619.2:n.8268+1G>A | |
| XM_006718843.4:c.8268+1G>A (ATM) | XP_006718906.1:n.8268+1G>A | |
| XM_006718845.2:c.4224+1G>A (ATM) | XP_006718908.1:n.4224+1G>A | |
| XM_011542840.3:c.8268+1G>A (ATM) | XP_011541142.1:n.8268+1G>A | |
| XM_011542842.3:c.8103+1G>A (ATM) | XP_011541144.1:n.8103+1G>A | |
| XM_011542843.2:c.8268+1G>A (ATM) | XP_011541145.1:n.8268+1G>A | |
| XM_011542844.3:c.7224+1G>A (ATM) | XP_011541146.1:n.7224+1G>A | |
| XM_011542845.2:c.6960+1G>A (ATM) | XP_011541147.1:n.6960+1G>A | |
| XM_017017789.2:c.8268+1G>A (ATM) | XP_016873278.1:n.8268+1G>A | |
| XM_017017790.2:c.8268+1G>A (ATM) | XP_016873279.1:n.8268+1G>A | |
| NM_001330368.2:c.641-26891C>T (C11orf65) | NP_001317297.1:n.641-26891C>T | |
| NM_001351110.2:c.695-670C>T (C11orf65) | NP_001338039.1:n.695-670C>T | |
| NM_001351834.2:c.8268+1G>A (ATM) | NP_001338763.1:n.8268+1G>A | |
| NM_000051.4:c.8268+1G>A (ATM) MANE Select | NP_000042.3:n.8268+1G>A | |
| NR_147053.3:n.2300-670C>T (C11orf65) |