Linked Data
ClinVar Variation Id:
1761881
ClinVar RCV Id:
RCV002419378
dbSNP Id:
rs2136658802
gnomAD v4:
11-108335034-A-G
MyVariant Identifiers:
chr11:g.108205761A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108335034A>G , CM000673.2:g.108335034A>G | GRCh38 |
| NC_000011.9:g.108205761A>G , CM000673.1:g.108205761A>G | GRCh37 |
| NC_000011.8:g.107710971A>G | NCBI36 |
| NG_009830.1:g.117203A>G , LRG_135:g.117203A>G | |
| NG_054724.1:g.139799T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.8076A>G (ATM) | ENSP00000388058.2:p.Leu2692= | |
| ENST00000713593.1:c.*7547A>G (ATM) | ENSP00000518889.1:n.*7547A>G | |
| ENST00000278616.9:c.8076A>G (ATM) | ENSP00000278616.4:p.Leu2692= | |
| ENST00000525056.2:n.2495A>G (ATM) | ||
| ENST00000638786.2:n.774A>G (ATM) | ||
| ENST00000682286.1:n.2833A>G (ATM) | ||
| ENST00000682302.1:n.2494A>G (ATM) | ||
| ENST00000683174.1:n.9560A>G (ATM) | ||
| ENST00000683524.1:n.3300A>G (ATM) | ||
| ENST00000684152.1:n.3492A>G (ATM) | ||
| ENST00000684180.1:n.550A>G (ATM) | ||
| ENST00000684447.1:n.4569A>G (ATM) | ||
| ENST00000527805.6:c.*3140A>G (ATM) | ENSP00000435747.2:n.*3140A>G | |
| ENST00000675595.1:c.*3211A>G (ATM) | ENSP00000502563.1:n.*3211A>G | |
| ENST00000675843.1:c.8076A>G (ATM) MANE Select | ENSP00000501606.1:p.Leu2692= | |
| ENST00000278616.8:c.8076A>G (ATM) | ENSP00000278616.4:p.Leu2692= | |
| ENST00000452508.6:c.8076A>G (ATM) | ENSP00000388058.2:p.Leu2692= | |
| ENST00000524755.5:c.299+186T>C (C11orf65) | ||
| ENST00000524792.5:n.4291A>G (ATM) | ||
| ENST00000525056.1:n.273A>G (ATM) | ||
| ENST00000525729.5:c.641-25963T>C (C11orf65) | ENSP00000433395.1:n.641-25963T>C | |
| ENST00000527531.5:c.*1269+186T>C (C11orf65) | ENSP00000431706.1:n.*1269+186T>C | |
| ENST00000533979.5:n.288A>G (ATM) | ||
| ENST00000615746.4:c.*1269+186T>C (C11orf65) | ENSP00000483537.1:n.*1269+186T>C | |
| NM_000051.3:c.8076A>G , LRG_135t1:c.8076A>G (ATM) | NP_000042.3:p.Leu2692= | |
| XM_005271414.3:c.*38+186T>C (C11orf65) | XP_005271471.1:n.*38+186T>C | |
| XM_005271415.3:c.804+186T>C (C11orf65) | XP_005271472.1:n.804+186T>C | |
| XM_005271561.3:c.8076A>G (ATM) | XP_005271618.2:p.Leu2692= | |
| XM_005271562.3:c.8076A>G (ATM) | XP_005271619.2:p.Leu2692= | |
| XM_006718843.2:c.8076A>G (ATM) | XP_006718906.1:p.Leu2692= | |
| XM_006718845.1:c.4032A>G (ATM) | XP_006718908.1:p.Leu1344= | |
| XM_011542840.1:c.8076A>G (ATM) | XP_011541142.1:p.Leu2692= | |
| XM_011542841.1:c.8076A>G (ATM) | XP_011541143.1:p.Leu2692= | |
| XM_011542842.1:c.7911A>G (ATM) | XP_011541144.1:p.Leu2637= | |
| XM_011542843.1:c.8076A>G (ATM) | XP_011541145.1:p.Leu2692= | |
| XM_011542844.1:c.7032A>G (ATM) | XP_011541146.1:p.Leu2344= | |
| XM_011542845.1:c.6768A>G (ATM) | XP_011541147.1:p.Leu2256= | |
| XM_011542847.1:c.3147A>G (ATM) | XP_011541149.1:p.Leu1049= | |
| NM_001330368.1:c.641-25963T>C (C11orf65) | NP_001317297.1:n.641-25963T>C | |
| NM_001351110.1:c.*38+186T>C (C11orf65) | NP_001338039.1:n.*38+186T>C | |
| NM_001351834.1:c.8076A>G (ATM) | NP_001338763.1:p.Leu2692= | |
| NR_147053.2:n.2374+186T>C (C11orf65) | ||
| XM_005271414.4:c.*38+186T>C (C11orf65) | XP_005271471.1:n.*38+186T>C | |
| XM_005271415.4:c.804+186T>C (C11orf65) | XP_005271472.1:n.804+186T>C | |
| XM_005271562.5:c.8076A>G (ATM) | XP_005271619.2:p.Leu2692= | |
| XM_006718843.4:c.8076A>G (ATM) | XP_006718906.1:p.Leu2692= | |
| XM_006718845.2:c.4032A>G (ATM) | XP_006718908.1:p.Leu1344= | |
| XM_011542840.3:c.8076A>G (ATM) | XP_011541142.1:p.Leu2692= | |
| XM_011542842.3:c.7911A>G (ATM) | XP_011541144.1:p.Leu2637= | |
| XM_011542843.2:c.8076A>G (ATM) | XP_011541145.1:p.Leu2692= | |
| XM_011542844.3:c.7032A>G (ATM) | XP_011541146.1:p.Leu2344= | |
| XM_011542845.2:c.6768A>G (ATM) | XP_011541147.1:p.Leu2256= | |
| XM_017017789.2:c.8076A>G (ATM) | XP_016873278.1:p.Leu2692= | |
| XM_017017790.2:c.8076A>G (ATM) | XP_016873279.1:p.Leu2692= | |
| NM_001330368.2:c.641-25963T>C (C11orf65) | NP_001317297.1:n.641-25963T>C | |
| NM_001351110.2:c.*38+186T>C (C11orf65) | NP_001338039.1:n.*38+186T>C | |
| NM_001351834.2:c.8076A>G (ATM) | NP_001338763.1:p.Leu2692= | |
| NM_000051.4:c.8076A>G (ATM) MANE Select | NP_000042.3:p.Leu2692= | |
| NR_147053.3:n.2372+186T>C (C11orf65) |