Linked Data
ClinVar Variation Id:
760083
dbSNP Id:
rs1591314147
MyVariant Identifiers:
chr11:g.108225562G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108354835G>T , CM000673.2:g.108354835G>T | GRCh38 |
| NC_000011.9:g.108225562G>T , CM000673.1:g.108225562G>T | GRCh37 |
| NC_000011.8:g.107730772G>T | NCBI36 |
| NG_009830.1:g.137004G>T , LRG_135:g.137004G>T | |
| NG_054724.1:g.119998C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000452508.7:c.8811G>T (ATM) | ENSP00000388058.2:p.Val2937= | |
| ENST00000713593.1:c.*8282G>T (ATM) | ENSP00000518889.1:n.*8282G>T | |
| ENST00000278616.9:c.8811G>T (ATM) | ENSP00000278616.4:p.Val2937= | |
| ENST00000638786.2:n.1509G>T (ATM) | ||
| ENST00000682286.1:n.3568G>T (ATM) | ||
| ENST00000682302.1:n.3229G>T (ATM) | ||
| ENST00000683174.1:n.10295G>T (ATM) | ||
| ENST00000683524.1:n.4035G>T (ATM) | ||
| ENST00000684152.1:n.4227G>T (ATM) | ||
| ENST00000684180.1:n.1285G>T (ATM) | ||
| ENST00000684447.1:n.5304G>T (ATM) | ||
| ENST00000527805.6:c.*3875G>T (ATM) | ENSP00000435747.2:n.*3875G>T | |
| ENST00000675595.1:c.*3946G>T (ATM) | ENSP00000502563.1:n.*3946G>T | |
| ENST00000675843.1:c.8811G>T (ATM) MANE Select | ENSP00000501606.1:p.Val2937= | |
| ENST00000278616.8:c.8811G>T (ATM) | ENSP00000278616.4:p.Val2937= | |
| ENST00000452508.6:c.8811G>T (ATM) | ENSP00000388058.2:p.Val2937= | |
| ENST00000524755.5:c.227-19543C>A (C11orf65) | ||
| ENST00000524792.5:n.5026G>T (ATM) | ||
| ENST00000525178.5:n.299G>T (ATM) | ||
| ENST00000525729.5:c.640+31085C>A (C11orf65) | ENSP00000433395.1:n.640+31085C>A | |
| ENST00000526725.1:n.272-14471C>A (C11orf65) | ||
| ENST00000527181.1:n.150G>T (ATM) | ||
| ENST00000527531.5:c.*1196+80C>A (C11orf65) | ENSP00000431706.1:n.*1196+80C>A | |
| ENST00000615746.4:c.*1196+80C>A (C11orf65) | ENSP00000483537.1:n.*1196+80C>A | |
| NM_000051.3:c.8811G>T , LRG_135t1:c.8811G>T (ATM) | NP_000042.3:p.Val2937= | |
| XM_005271414.3:c.788-19543C>A (C11orf65) | XP_005271471.1:n.788-19543C>A | |
| XM_005271415.3:c.732-19543C>A (C11orf65) | XP_005271472.1:n.732-19543C>A | |
| XM_005271561.3:c.8811G>T (ATM) | XP_005271618.2:p.Val2937= | |
| XM_005271562.3:c.8811G>T (ATM) | XP_005271619.2:p.Val2937= | |
| XM_006718843.2:c.8811G>T (ATM) | XP_006718906.1:p.Val2937= | |
| XM_006718845.1:c.4767G>T (ATM) | XP_006718908.1:p.Val1589= | |
| XM_011542640.1:c.788-14471C>A (C11orf65) | XP_011540942.1:n.788-14471C>A | |
| XM_011542642.1:c.732-5762C>A (C11orf65) | XP_011540944.1:n.732-5762C>A | |
| XM_011542643.1:c.732-14471C>A (C11orf65) | XP_011540945.1:n.732-14471C>A | |
| XM_011542840.1:c.8811G>T (ATM) | XP_011541142.1:p.Val2937= | |
| XM_011542841.1:c.8811G>T (ATM) | XP_011541143.1:p.Val2937= | |
| XM_011542842.1:c.8646G>T (ATM) | XP_011541144.1:p.Val2882= | |
| XM_011542844.1:c.7767G>T (ATM) | XP_011541146.1:p.Val2589= | |
| XM_011542845.1:c.7503G>T (ATM) | XP_011541147.1:p.Val2501= | |
| XM_011542847.1:c.3882G>T (ATM) | XP_011541149.1:p.Val1294= | |
| NM_001330368.1:c.640+31085C>A (C11orf65) | NP_001317297.1:n.640+31085C>A | |
| NM_001351110.1:c.695-19543C>A (C11orf65) | NP_001338039.1:n.695-19543C>A | |
| NM_001351834.1:c.8811G>T (ATM) | NP_001338763.1:p.Val2937= | |
| NR_147053.2:n.2301+80C>A (C11orf65) | ||
| XM_005271414.4:c.788-19543C>A (C11orf65) | XP_005271471.1:n.788-19543C>A | |
| XM_005271415.4:c.732-19543C>A (C11orf65) | XP_005271472.1:n.732-19543C>A | |
| XM_005271562.5:c.8811G>T (ATM) | XP_005271619.2:p.Val2937= | |
| XM_006718843.4:c.8811G>T (ATM) | XP_006718906.1:p.Val2937= | |
| XM_006718845.2:c.4767G>T (ATM) | XP_006718908.1:p.Val1589= | |
| XM_011542640.2:c.788-14471C>A (C11orf65) | XP_011540942.1:n.788-14471C>A | |
| XM_011542643.2:c.732-14471C>A (C11orf65) | XP_011540945.1:n.732-14471C>A | |
| XM_011542840.3:c.8811G>T (ATM) | XP_011541142.1:p.Val2937= | |
| XM_011542842.3:c.8646G>T (ATM) | XP_011541144.1:p.Val2882= | |
| XM_011542844.3:c.7767G>T (ATM) | XP_011541146.1:p.Val2589= | |
| XM_011542845.2:c.7503G>T (ATM) | XP_011541147.1:p.Val2501= | |
| XM_017017247.1:c.904-14471C>A (C11orf65) | XP_016872736.1:n.904-14471C>A | |
| XM_017017789.2:c.8811G>T (ATM) | XP_016873278.1:p.Val2937= | |
| XM_017017790.2:c.8811G>T (ATM) | XP_016873279.1:p.Val2937= | |
| NM_001330368.2:c.640+31085C>A (C11orf65) | NP_001317297.1:n.640+31085C>A | |
| NM_001351110.2:c.695-19543C>A (C11orf65) | NP_001338039.1:n.695-19543C>A | |
| NM_001351834.2:c.8811G>T (ATM) | NP_001338763.1:p.Val2937= | |
| NM_000051.4:c.8811G>T (ATM) MANE Select | NP_000042.3:p.Val2937= | |
| NR_147053.3:n.2299+80C>A (C11orf65) |