Revel Score:
ENST00000278616
0.113
ENST00000452508
0.113
gnomAD v2:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108365190G>T , CM000673.2:g.108365190G>T | GRCh38 |
| NC_000011.9:g.108235917G>T , CM000673.1:g.108235917G>T | GRCh37 |
| NC_000011.8:g.107741127G>T | NCBI36 |
| NG_009830.1:g.147359G>T , LRG_135:g.147359G>T | |
| NG_054724.1:g.109643C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.8959G>T (ATM) | ENSP00000388058.2:p.Asp2987Tyr | |
| ENST00000713593.1:c.*8430G>T (ATM) | ENSP00000518889.1:n.*8430G>T | |
| ENST00000278616.9:c.8959G>T (ATM) | ENSP00000278616.4:p.Asp2987Tyr | |
| ENST00000638786.2:n.1657G>T (ATM) | ||
| ENST00000682286.1:n.3716G>T (ATM) | ||
| ENST00000682302.1:n.3377G>T (ATM) | ||
| ENST00000682569.1:n.2306G>T (ATM) | ||
| ENST00000683174.1:n.10443G>T (ATM) | ||
| ENST00000683524.1:n.4183G>T (ATM) | ||
| ENST00000684152.1:n.4375G>T (ATM) | ||
| ENST00000684180.1:n.1433G>T (ATM) | ||
| ENST00000684447.1:n.5452G>T (ATM) | ||
| ENST00000527805.6:c.*4023G>T (ATM) | ENSP00000435747.2:n.*4023G>T | |
| ENST00000675595.1:c.*4094G>T (ATM) | ENSP00000502563.1:n.*4094G>T | |
| ENST00000675843.1:c.8959G>T (ATM) MANE Select | ENSP00000501606.1:p.Asp2987Tyr | |
| ENST00000278616.8:c.8959G>T (ATM) | ENSP00000278616.4:p.Asp2987Tyr | |
| ENST00000452508.6:c.8959G>T (ATM) | ENSP00000388058.2:p.Asp2987Tyr | |
| ENST00000524755.5:c.226+28018C>A (C11orf65) | ||
| ENST00000524792.5:n.5174G>T (ATM) | ||
| ENST00000525178.5:n.447G>T (ATM) | ||
| ENST00000525729.5:c.640+20730C>A (C11orf65) | ENSP00000433395.1:n.640+20730C>A | |
| ENST00000526725.1:n.272-24826C>A (C11orf65) | ||
| ENST00000527181.1:n.298G>T (ATM) | ||
| ENST00000527531.5:c.*2-9081C>A (C11orf65) | ENSP00000431706.1:n.*2-9081C>A | |
| ENST00000615746.4:c.*2-9081C>A (C11orf65) | ENSP00000483537.1:n.*2-9081C>A | |
| NM_000051.3:c.8959G>T , LRG_135t1:c.8959G>T (ATM) | NP_000042.3:p.Asp2987Tyr | |
| XM_005271414.3:c.787+20730C>A (C11orf65) | XP_005271471.1:n.787+20730C>A | |
| XM_005271415.3:c.731+28018C>A (C11orf65) | XP_005271472.1:n.731+28018C>A | |
| XM_005271561.3:c.8959G>T (ATM) | XP_005271618.2:p.Asp2987Tyr | |
| XM_005271562.3:c.8959G>T (ATM) | XP_005271619.2:p.Asp2987Tyr | |
| XM_006718843.2:c.8959G>T (ATM) | XP_006718906.1:p.Asp2987Tyr | |
| XM_006718845.1:c.4915G>T (ATM) | XP_006718908.1:p.Asp1639Tyr | |
| XM_011542640.1:c.787+20730C>A (C11orf65) | XP_011540942.1:n.787+20730C>A | |
| XM_011542642.1:c.732-16117C>A (C11orf65) | XP_011540944.1:n.732-16117C>A | |
| XM_011542643.1:c.732-24826C>A (C11orf65) | XP_011540945.1:n.732-24826C>A | |
| XM_011542840.1:c.8959G>T (ATM) | XP_011541142.1:p.Asp2987Tyr | |
| XM_011542841.1:c.8959G>T (ATM) | XP_011541143.1:p.Asp2987Tyr | |
| XM_011542842.1:c.8794G>T (ATM) | XP_011541144.1:p.Asp2932Tyr | |
| XM_011542844.1:c.7915G>T (ATM) | XP_011541146.1:p.Asp2639Tyr | |
| XM_011542845.1:c.7651G>T (ATM) | XP_011541147.1:p.Asp2551Tyr | |
| XM_011542847.1:c.4030G>T (ATM) | XP_011541149.1:p.Asp1344Tyr | |
| NM_001330368.1:c.640+20730C>A (C11orf65) | NP_001317297.1:n.640+20730C>A | |
| NM_001351110.1:c.694+20730C>A (C11orf65) | NP_001338039.1:n.694+20730C>A | |
| NM_001351834.1:c.8959G>T (ATM) | NP_001338763.1:p.Asp2987Tyr | |
| NR_147053.2:n.1107-9081C>A (C11orf65) | ||
| XM_005271414.4:c.787+20730C>A (C11orf65) | XP_005271471.1:n.787+20730C>A | |
| XM_005271415.4:c.731+28018C>A (C11orf65) | XP_005271472.1:n.731+28018C>A | |
| XM_005271562.5:c.8959G>T (ATM) | XP_005271619.2:p.Asp2987Tyr | |
| XM_006718843.4:c.8959G>T (ATM) | XP_006718906.1:p.Asp2987Tyr | |
| XM_006718845.2:c.4915G>T (ATM) | XP_006718908.1:p.Asp1639Tyr | |
| XM_011542640.2:c.787+20730C>A (C11orf65) | XP_011540942.1:n.787+20730C>A | |
| XM_011542643.2:c.732-24826C>A (C11orf65) | XP_011540945.1:n.732-24826C>A | |
| XM_011542840.3:c.8959G>T (ATM) | XP_011541142.1:p.Asp2987Tyr | |
| XM_011542842.3:c.8794G>T (ATM) | XP_011541144.1:p.Asp2932Tyr | |
| XM_011542844.3:c.7915G>T (ATM) | XP_011541146.1:p.Asp2639Tyr | |
| XM_011542845.2:c.7651G>T (ATM) | XP_011541147.1:p.Asp2551Tyr | |
| XM_017017247.1:c.903+17870C>A (C11orf65) | XP_016872736.1:n.903+17870C>A | |
| XM_017017789.2:c.8959G>T (ATM) | XP_016873278.1:p.Asp2987Tyr | |
| XM_017017790.2:c.8959G>T (ATM) | XP_016873279.1:p.Asp2987Tyr | |
| NM_001330368.2:c.640+20730C>A (C11orf65) | NP_001317297.1:n.640+20730C>A | |
| NM_001351110.2:c.694+20730C>A (C11orf65) | NP_001338039.1:n.694+20730C>A | |
| NM_001351834.2:c.8959G>T (ATM) | NP_001338763.1:p.Asp2987Tyr | |
| NM_000051.4:c.8959G>T (ATM) MANE Select | NP_000042.3:p.Asp2987Tyr | |
| NR_147053.3:n.1105-9081C>A (C11orf65) |