Linked Data
ClinVar Variation Id:
481124
dbSNP Id:
rs1342227995
gnomAD v2:
11-108188252-A-G
gnomAD v4:
11-108317525-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108317525A>G , CM000673.2:g.108317525A>G | GRCh38 |
| NC_000011.9:g.108188252A>G , CM000673.1:g.108188252A>G | GRCh37 |
| NC_000011.8:g.107693462A>G | NCBI36 |
| NG_009830.1:g.99694A>G , LRG_135:g.99694A>G | |
| NG_054724.1:g.157308T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.6347+4A>G (ATM) | ENSP00000388058.2:n.6347+4A>G | |
| ENST00000713593.1:c.*5818+4A>G (ATM) | ENSP00000518889.1:n.*5818+4A>G | |
| ENST00000278616.9:c.6347+4A>G (ATM) | ENSP00000278616.4:n.6347+4A>G | |
| ENST00000525056.2:n.766+4A>G (ATM) | ||
| ENST00000682286.1:n.1104+4A>G (ATM) | ||
| ENST00000682302.1:n.765+4A>G (ATM) | ||
| ENST00000683174.1:n.7831+4A>G (ATM) | ||
| ENST00000683524.1:n.1571+4A>G (ATM) | ||
| ENST00000684152.1:n.2061+4A>G (ATM) | ||
| ENST00000527805.6:c.*1411+4A>G (ATM) | ENSP00000435747.2:n.*1411+4A>G | |
| ENST00000675595.1:c.*1411+4A>G (ATM) | ENSP00000502563.1:n.*1411+4A>G | |
| ENST00000675843.1:c.6347+4A>G (ATM) MANE Select | ENSP00000501606.1:n.6347+4A>G | |
| ENST00000278616.8:c.6347+4A>G (ATM) | ENSP00000278616.4:n.6347+4A>G | |
| ENST00000452508.6:c.6347+4A>G (ATM) | ENSP00000388058.2:n.6347+4A>G | |
| ENST00000524792.5:n.2562+4A>G (ATM) | ||
| ENST00000525729.5:c.641-8454T>C (C11orf65) | ENSP00000433395.1:n.641-8454T>C | |
| ENST00000533690.5:n.1751+4A>G (ATM) | ||
| NM_000051.3:c.6347+4A>G , LRG_135t1:c.6347+4A>G (ATM) | NP_000042.3:n.6347+4A>G | |
| XM_005271561.3:c.6347+4A>G (ATM) | XP_005271618.2:n.6347+4A>G | |
| XM_005271562.3:c.6347+4A>G (ATM) | XP_005271619.2:n.6347+4A>G | |
| XM_006718843.2:c.6347+4A>G (ATM) | XP_006718906.1:n.6347+4A>G | |
| XM_006718845.1:c.2303+4A>G (ATM) | XP_006718908.1:n.2303+4A>G | |
| XM_011542840.1:c.6347+4A>G (ATM) | XP_011541142.1:n.6347+4A>G | |
| XM_011542841.1:c.6347+4A>G (ATM) | XP_011541143.1:n.6347+4A>G | |
| XM_011542842.1:c.6182+4A>G (ATM) | XP_011541144.1:n.6182+4A>G | |
| XM_011542843.1:c.6347+4A>G (ATM) | XP_011541145.1:n.6347+4A>G | |
| XM_011542844.1:c.5303+4A>G (ATM) | XP_011541146.1:n.5303+4A>G | |
| XM_011542845.1:c.5039+4A>G (ATM) | XP_011541147.1:n.5039+4A>G | |
| XM_011542847.1:c.1418+4A>G (ATM) | XP_011541149.1:n.1418+4A>G | |
| NM_001330368.1:c.641-8454T>C (C11orf65) | NP_001317297.1:n.641-8454T>C | |
| NM_001351110.1:c.*39-8454T>C (C11orf65) | NP_001338039.1:n.*39-8454T>C | |
| NM_001351834.1:c.6347+4A>G (ATM) | NP_001338763.1:n.6347+4A>G | |
| XM_005271562.5:c.6347+4A>G (ATM) | XP_005271619.2:n.6347+4A>G | |
| XM_006718843.4:c.6347+4A>G (ATM) | XP_006718906.1:n.6347+4A>G | |
| XM_006718845.2:c.2303+4A>G (ATM) | XP_006718908.1:n.2303+4A>G | |
| XM_011542840.3:c.6347+4A>G (ATM) | XP_011541142.1:n.6347+4A>G | |
| XM_011542842.3:c.6182+4A>G (ATM) | XP_011541144.1:n.6182+4A>G | |
| XM_011542843.2:c.6347+4A>G (ATM) | XP_011541145.1:n.6347+4A>G | |
| XM_011542844.3:c.5303+4A>G (ATM) | XP_011541146.1:n.5303+4A>G | |
| XM_011542845.2:c.5039+4A>G (ATM) | XP_011541147.1:n.5039+4A>G | |
| XM_017017789.2:c.6347+4A>G (ATM) | XP_016873278.1:n.6347+4A>G | |
| XM_017017790.2:c.6347+4A>G (ATM) | XP_016873279.1:n.6347+4A>G | |
| XM_017017791.1:c.6347+4A>G (ATM) | XP_016873280.1:n.6347+4A>G | |
| NM_001330368.2:c.641-8454T>C (C11orf65) | NP_001317297.1:n.641-8454T>C | |
| NM_001351110.2:c.*39-8454T>C (C11orf65) | NP_001338039.1:n.*39-8454T>C | |
| NM_001351834.2:c.6347+4A>G (ATM) | NP_001338763.1:n.6347+4A>G | |
| NM_000051.4:c.6347+4A>G (ATM) MANE Select | NP_000042.3:n.6347+4A>G |