Linked Data
ClinVar Variation Id:
141676
dbSNP Id:
rs556778314
ExAC:
11:108196952 G / A
gnomAD v2:
11-108196952-G-A
gnomAD v3:
11-108326225-G-A
gnomAD v4:
11-108326225-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108326225G>A , CM000673.2:g.108326225G>A | GRCh38 |
| NC_000011.9:g.108196952G>A , CM000673.1:g.108196952G>A | GRCh37 |
| NC_000011.8:g.107702162G>A | NCBI36 |
| NG_009830.1:g.108394G>A , LRG_135:g.108394G>A | |
| NG_054724.1:g.148608C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.6975G>A (ATM) | ENSP00000388058.2:p.Ala2325= | |
| ENST00000713593.1:c.*6446G>A (ATM) | ENSP00000518889.1:n.*6446G>A | |
| ENST00000278616.9:c.6975G>A (ATM) | ENSP00000278616.4:p.Ala2325= | |
| ENST00000525056.2:n.1394G>A (ATM) | ||
| ENST00000682286.1:n.1732G>A (ATM) | ||
| ENST00000682302.1:n.1393G>A (ATM) | ||
| ENST00000683174.1:n.8459G>A (ATM) | ||
| ENST00000683524.1:n.2199G>A (ATM) | ||
| ENST00000684152.1:n.2689G>A (ATM) | ||
| ENST00000684447.1:n.19G>A (ATM) | ||
| ENST00000527805.6:c.*2039G>A (ATM) | ENSP00000435747.2:n.*2039G>A | |
| ENST00000675595.1:c.*2110G>A (ATM) | ENSP00000502563.1:n.*2110G>A | |
| ENST00000675843.1:c.6975G>A (ATM) MANE Select | ENSP00000501606.1:p.Ala2325= | |
| ENST00000278616.8:c.6975G>A (ATM) | ENSP00000278616.4:p.Ala2325= | |
| ENST00000452508.6:c.6975G>A (ATM) | ENSP00000388058.2:p.Ala2325= | |
| ENST00000524792.5:n.3190G>A (ATM) | ||
| ENST00000525729.5:c.641-17154C>T (C11orf65) | ENSP00000433395.1:n.641-17154C>T | |
| ENST00000533690.5:n.2379G>A (ATM) | ||
| NM_000051.3:c.6975G>A , LRG_135t1:c.6975G>A (ATM) | NP_000042.3:p.Ala2325= | |
| XM_005271561.3:c.6975G>A (ATM) | XP_005271618.2:p.Ala2325= | |
| XM_005271562.3:c.6975G>A (ATM) | XP_005271619.2:p.Ala2325= | |
| XM_006718843.2:c.6975G>A (ATM) | XP_006718906.1:p.Ala2325= | |
| XM_006718845.1:c.2931G>A (ATM) | XP_006718908.1:p.Ala977= | |
| XM_011542840.1:c.6975G>A (ATM) | XP_011541142.1:p.Ala2325= | |
| XM_011542841.1:c.6975G>A (ATM) | XP_011541143.1:p.Ala2325= | |
| XM_011542842.1:c.6810G>A (ATM) | XP_011541144.1:p.Ala2270= | |
| XM_011542843.1:c.6975G>A (ATM) | XP_011541145.1:p.Ala2325= | |
| XM_011542844.1:c.5931G>A (ATM) | XP_011541146.1:p.Ala1977= | |
| XM_011542845.1:c.5667G>A (ATM) | XP_011541147.1:p.Ala1889= | |
| XM_011542847.1:c.2046G>A (ATM) | XP_011541149.1:p.Ala682= | |
| NM_001330368.1:c.641-17154C>T (C11orf65) | NP_001317297.1:n.641-17154C>T | |
| NM_001351110.1:c.*38+8995C>T (C11orf65) | NP_001338039.1:n.*38+8995C>T | |
| NM_001351834.1:c.6975G>A (ATM) | NP_001338763.1:p.Ala2325= | |
| XM_005271562.5:c.6975G>A (ATM) | XP_005271619.2:p.Ala2325= | |
| XM_006718843.4:c.6975G>A (ATM) | XP_006718906.1:p.Ala2325= | |
| XM_006718845.2:c.2931G>A (ATM) | XP_006718908.1:p.Ala977= | |
| XM_011542840.3:c.6975G>A (ATM) | XP_011541142.1:p.Ala2325= | |
| XM_011542842.3:c.6810G>A (ATM) | XP_011541144.1:p.Ala2270= | |
| XM_011542843.2:c.6975G>A (ATM) | XP_011541145.1:p.Ala2325= | |
| XM_011542844.3:c.5931G>A (ATM) | XP_011541146.1:p.Ala1977= | |
| XM_011542845.2:c.5667G>A (ATM) | XP_011541147.1:p.Ala1889= | |
| XM_017017789.2:c.6975G>A (ATM) | XP_016873278.1:p.Ala2325= | |
| XM_017017790.2:c.6975G>A (ATM) | XP_016873279.1:p.Ala2325= | |
| NM_001330368.2:c.641-17154C>T (C11orf65) | NP_001317297.1:n.641-17154C>T | |
| NM_001351110.2:c.*38+8995C>T (C11orf65) | NP_001338039.1:n.*38+8995C>T | |
| NM_001351834.2:c.6975G>A (ATM) | NP_001338763.1:p.Ala2325= | |
| NM_000051.4:c.6975G>A (ATM) MANE Select | NP_000042.3:p.Ala2325= |