Linked Data
ClinVar Variation Id:
1760646
ClinVar RCV Id:
RCV002409865
dbSNP Id:
rs138941496
MyVariant Identifiers:
chr11:g.108203492C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108332765C>A , CM000673.2:g.108332765C>A | GRCh38 |
| NC_000011.9:g.108203492C>A , CM000673.1:g.108203492C>A | GRCh37 |
| NC_000011.8:g.107708702C>A | NCBI36 |
| NG_009830.1:g.114934C>A , LRG_135:g.114934C>A | |
| NG_054724.1:g.142068G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.7792C>A (ATM) | ENSP00000388058.2:p.Arg2598= | |
| ENST00000713593.1:c.*7263C>A (ATM) | ENSP00000518889.1:n.*7263C>A | |
| ENST00000278616.9:c.7792C>A (ATM) | ENSP00000278616.4:p.Arg2598= | |
| ENST00000525056.2:n.2211C>A (ATM) | ||
| ENST00000525537.3:n.1473C>A (ATM) | ||
| ENST00000638786.2:n.625+728C>A (ATM) | ||
| ENST00000682286.1:n.2549C>A (ATM) | ||
| ENST00000682302.1:n.2210C>A (ATM) | ||
| ENST00000683174.1:n.9276C>A (ATM) | ||
| ENST00000683524.1:n.3016C>A (ATM) | ||
| ENST00000684152.1:n.3344-1121C>A (ATM) | ||
| ENST00000684180.1:n.266C>A (ATM) | ||
| ENST00000684447.1:n.3300C>A (ATM) | ||
| ENST00000527805.6:c.*2856C>A (ATM) | ENSP00000435747.2:n.*2856C>A | |
| ENST00000675595.1:c.*2927C>A (ATM) | ENSP00000502563.1:n.*2927C>A | |
| ENST00000675843.1:c.7792C>A (ATM) MANE Select | ENSP00000501606.1:p.Arg2598= | |
| ENST00000278616.8:c.7792C>A (ATM) | ENSP00000278616.4:p.Arg2598= | |
| ENST00000452508.6:c.7792C>A (ATM) | ENSP00000388058.2:p.Arg2598= | |
| ENST00000524755.5:c.300-1198G>T (C11orf65) | ||
| ENST00000524792.5:n.4007C>A (ATM) | ||
| ENST00000525729.5:c.641-23694G>T (C11orf65) | ENSP00000433395.1:n.641-23694G>T | |
| ENST00000527531.5:c.*1270-1198G>T (C11orf65) | ENSP00000431706.1:n.*1270-1198G>T | |
| ENST00000533690.5:n.3196C>A (ATM) | ||
| ENST00000533979.5:n.4C>A (ATM) | ||
| ENST00000615746.4:c.*1270-1198G>T (C11orf65) | ENSP00000483537.1:n.*1270-1198G>T | |
| NM_000051.3:c.7792C>A , LRG_135t1:c.7792C>A (ATM) | NP_000042.3:p.Arg2598= | |
| XM_005271414.3:c.*39-1198G>T (C11orf65) | XP_005271471.1:n.*39-1198G>T | |
| XM_005271415.3:c.805-1198G>T (C11orf65) | XP_005271472.1:n.805-1198G>T | |
| XM_005271561.3:c.7792C>A (ATM) | XP_005271618.2:p.Arg2598= | |
| XM_005271562.3:c.7792C>A (ATM) | XP_005271619.2:p.Arg2598= | |
| XM_006718843.2:c.7792C>A (ATM) | XP_006718906.1:p.Arg2598= | |
| XM_006718845.1:c.3748C>A (ATM) | XP_006718908.1:p.Arg1250= | |
| XM_011542840.1:c.7792C>A (ATM) | XP_011541142.1:p.Arg2598= | |
| XM_011542841.1:c.7792C>A (ATM) | XP_011541143.1:p.Arg2598= | |
| XM_011542842.1:c.7627C>A (ATM) | XP_011541144.1:p.Arg2543= | |
| XM_011542843.1:c.7792C>A (ATM) | XP_011541145.1:p.Arg2598= | |
| XM_011542844.1:c.6748C>A (ATM) | XP_011541146.1:p.Arg2250= | |
| XM_011542845.1:c.6484C>A (ATM) | XP_011541147.1:p.Arg2162= | |
| XM_011542847.1:c.2863C>A (ATM) | XP_011541149.1:p.Arg955= | |
| NM_001330368.1:c.641-23694G>T (C11orf65) | NP_001317297.1:n.641-23694G>T | |
| NM_001351110.1:c.*38+2455G>T (C11orf65) | NP_001338039.1:n.*38+2455G>T | |
| NM_001351834.1:c.7792C>A (ATM) | NP_001338763.1:p.Arg2598= | |
| NR_147053.2:n.2375-1198G>T (C11orf65) | ||
| XM_005271414.4:c.*39-1198G>T (C11orf65) | XP_005271471.1:n.*39-1198G>T | |
| XM_005271415.4:c.805-1198G>T (C11orf65) | XP_005271472.1:n.805-1198G>T | |
| XM_005271562.5:c.7792C>A (ATM) | XP_005271619.2:p.Arg2598= | |
| XM_006718843.4:c.7792C>A (ATM) | XP_006718906.1:p.Arg2598= | |
| XM_006718845.2:c.3748C>A (ATM) | XP_006718908.1:p.Arg1250= | |
| XM_011542840.3:c.7792C>A (ATM) | XP_011541142.1:p.Arg2598= | |
| XM_011542842.3:c.7627C>A (ATM) | XP_011541144.1:p.Arg2543= | |
| XM_011542843.2:c.7792C>A (ATM) | XP_011541145.1:p.Arg2598= | |
| XM_011542844.3:c.6748C>A (ATM) | XP_011541146.1:p.Arg2250= | |
| XM_011542845.2:c.6484C>A (ATM) | XP_011541147.1:p.Arg2162= | |
| XM_017017789.2:c.7792C>A (ATM) | XP_016873278.1:p.Arg2598= | |
| XM_017017790.2:c.7792C>A (ATM) | XP_016873279.1:p.Arg2598= | |
| NM_001330368.2:c.641-23694G>T (C11orf65) | NP_001317297.1:n.641-23694G>T | |
| NM_001351110.2:c.*38+2455G>T (C11orf65) | NP_001338039.1:n.*38+2455G>T | |
| NM_001351834.2:c.7792C>A (ATM) | NP_001338763.1:p.Arg2598= | |
| NM_000051.4:c.7792C>A (ATM) MANE Select | NP_000042.3:p.Arg2598= | |
| NR_147053.3:n.2373-1198G>T (C11orf65) |