Revel Score:
ENST00000278616
0.816
ENST00000452508
0.816
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108310255C>G , CM000673.2:g.108310255C>G | GRCh38 |
| NC_000011.9:g.108180982C>G , CM000673.1:g.108180982C>G | GRCh37 |
| NC_000011.8:g.107686192C>G | NCBI36 |
| NG_009830.1:g.92424C>G , LRG_135:g.92424C>G | |
| NG_054724.1:g.164578G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.5858C>G (ATM) | ENSP00000388058.2:p.Thr1953Arg | |
| ENST00000713593.1:c.*5329C>G (ATM) | ENSP00000518889.1:n.*5329C>G | |
| ENST00000278616.9:c.5858C>G (ATM) | ENSP00000278616.4:p.Thr1953Arg | |
| ENST00000525056.2:n.277C>G (ATM) | ||
| ENST00000682286.1:n.615C>G (ATM) | ||
| ENST00000682302.1:n.276C>G (ATM) | ||
| ENST00000683174.1:n.7342C>G (ATM) | ||
| ENST00000683524.1:n.1082C>G (ATM) | ||
| ENST00000684152.1:n.1572C>G (ATM) | ||
| ENST00000527805.6:c.*922C>G (ATM) | ENSP00000435747.2:n.*922C>G | |
| ENST00000675595.1:c.*922C>G (ATM) | ENSP00000502563.1:n.*922C>G | |
| ENST00000675843.1:c.5858C>G (ATM) MANE Select | ENSP00000501606.1:p.Thr1953Arg | |
| ENST00000278616.8:c.5858C>G (ATM) | ENSP00000278616.4:p.Thr1953Arg | |
| ENST00000452508.6:c.5858C>G (ATM) | ENSP00000388058.2:p.Thr1953Arg | |
| ENST00000524792.5:n.2073C>G (ATM) | ||
| ENST00000525729.5:c.641-1184G>C (C11orf65) | ENSP00000433395.1:n.641-1184G>C | |
| ENST00000529588.5:c.282C>G (ATM) | ||
| ENST00000532765.1:n.175C>G (ATM) | ||
| ENST00000533690.5:n.1262C>G (ATM) | ||
| NM_000051.3:c.5858C>G , LRG_135t1:c.5858C>G (ATM) | NP_000042.3:p.Thr1953Arg | |
| XM_005271561.3:c.5858C>G (ATM) | XP_005271618.2:p.Thr1953Arg | |
| XM_005271562.3:c.5858C>G (ATM) | XP_005271619.2:p.Thr1953Arg | |
| XM_006718843.2:c.5858C>G (ATM) | XP_006718906.1:p.Thr1953Arg | |
| XM_006718845.1:c.1814C>G (ATM) | XP_006718908.1:p.Thr605Arg | |
| XM_011542840.1:c.5858C>G (ATM) | XP_011541142.1:p.Thr1953Arg | |
| XM_011542841.1:c.5858C>G (ATM) | XP_011541143.1:p.Thr1953Arg | |
| XM_011542842.1:c.5693C>G (ATM) | XP_011541144.1:p.Thr1898Arg | |
| XM_011542843.1:c.5858C>G (ATM) | XP_011541145.1:p.Thr1953Arg | |
| XM_011542844.1:c.4814C>G (ATM) | XP_011541146.1:p.Thr1605Arg | |
| XM_011542845.1:c.4550C>G (ATM) | XP_011541147.1:p.Thr1517Arg | |
| XM_011542847.1:c.929C>G (ATM) | XP_011541149.1:p.Thr310Arg | |
| NM_001330368.1:c.641-1184G>C (C11orf65) | NP_001317297.1:n.641-1184G>C | |
| NM_001351110.1:c.*39-1184G>C (C11orf65) | NP_001338039.1:n.*39-1184G>C | |
| NM_001351834.1:c.5858C>G (ATM) | NP_001338763.1:p.Thr1953Arg | |
| XM_005271562.5:c.5858C>G (ATM) | XP_005271619.2:p.Thr1953Arg | |
| XM_006718843.4:c.5858C>G (ATM) | XP_006718906.1:p.Thr1953Arg | |
| XM_006718845.2:c.1814C>G (ATM) | XP_006718908.1:p.Thr605Arg | |
| XM_011542840.3:c.5858C>G (ATM) | XP_011541142.1:p.Thr1953Arg | |
| XM_011542842.3:c.5693C>G (ATM) | XP_011541144.1:p.Thr1898Arg | |
| XM_011542843.2:c.5858C>G (ATM) | XP_011541145.1:p.Thr1953Arg | |
| XM_011542844.3:c.4814C>G (ATM) | XP_011541146.1:p.Thr1605Arg | |
| XM_011542845.2:c.4550C>G (ATM) | XP_011541147.1:p.Thr1517Arg | |
| XM_017017789.2:c.5858C>G (ATM) | XP_016873278.1:p.Thr1953Arg | |
| XM_017017790.2:c.5858C>G (ATM) | XP_016873279.1:p.Thr1953Arg | |
| XM_017017791.1:c.5858C>G (ATM) | XP_016873280.1:p.Thr1953Arg | |
| XR_002957150.1:n.6458C>G (ATM) | ||
| NM_001330368.2:c.641-1184G>C (C11orf65) | NP_001317297.1:n.641-1184G>C | |
| NM_001351110.2:c.*39-1184G>C (C11orf65) | NP_001338039.1:n.*39-1184G>C | |
| NM_001351834.2:c.5858C>G (ATM) | NP_001338763.1:p.Thr1953Arg | |
| NM_000051.4:c.5858C>G (ATM) MANE Select | NP_000042.3:p.Thr1953Arg |