Linked Data
ClinVar Variation Id:
181839
ClinVar RCV Id:
RCV000159594
RCV000212070
RCV000205045
RCV000589020
RCV001356383
RCV003492636
RCV004551364
dbSNP Id:
rs34393781
ExAC:
11:108201127 T / C
gnomAD v2:
11-108201127-T-C
gnomAD v3:
11-108330400-T-C
gnomAD v4:
11-108330400-T-C
MyVariant Identifiers:
chr11:g.108201127T>C (hg19)
chr11:g.108201127_108201131delinsCGAAG (hg19)
chr11:g.108330400T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108330400T>C , CM000673.2:g.108330400T>C | GRCh38 |
| NC_000011.9:g.108201127T>C , CM000673.1:g.108201127T>C | GRCh37 |
| NC_000011.8:g.107706337T>C | NCBI36 |
| NG_009830.1:g.112569T>C , LRG_135:g.112569T>C | |
| NG_054724.1:g.144433A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.7494T>C (ATM) | ENSP00000388058.2:p.Ser2498= | |
| ENST00000713593.1:c.*6965T>C (ATM) | ENSP00000518889.1:n.*6965T>C | |
| ENST00000278616.9:c.7494T>C (ATM) | ENSP00000278616.4:p.Ser2498= | |
| ENST00000525056.2:n.1913T>C (ATM) | ||
| ENST00000525537.3:n.451T>C (ATM) | ||
| ENST00000638786.2:n.331T>C (ATM) | ||
| ENST00000682286.1:n.2251T>C (ATM) | ||
| ENST00000682302.1:n.1912T>C (ATM) | ||
| ENST00000683174.1:n.8978T>C (ATM) | ||
| ENST00000683524.1:n.2718T>C (ATM) | ||
| ENST00000684152.1:n.3208T>C (ATM) | ||
| ENST00000684447.1:n.1957T>C (ATM) | ||
| ENST00000527805.6:c.*2558T>C (ATM) | ENSP00000435747.2:n.*2558T>C | |
| ENST00000675595.1:c.*2629T>C (ATM) | ENSP00000502563.1:n.*2629T>C | |
| ENST00000675843.1:c.7494T>C (ATM) MANE Select | ENSP00000501606.1:p.Ser2498= | |
| ENST00000278616.8:c.7494T>C (ATM) | ENSP00000278616.4:p.Ser2498= | |
| ENST00000452508.6:c.7494T>C (ATM) | ENSP00000388058.2:p.Ser2498= | |
| ENST00000524792.5:n.3709T>C (ATM) | ||
| ENST00000525729.5:c.641-21329A>G (C11orf65) | ENSP00000433395.1:n.641-21329A>G | |
| ENST00000533690.5:n.2898T>C (ATM) | ||
| NM_000051.3:c.7494T>C , LRG_135t1:c.7494T>C (ATM) | NP_000042.3:p.Ser2498= | |
| XM_005271561.3:c.7494T>C (ATM) | XP_005271618.2:p.Ser2498= | |
| XM_005271562.3:c.7494T>C (ATM) | XP_005271619.2:p.Ser2498= | |
| XM_006718843.2:c.7494T>C (ATM) | XP_006718906.1:p.Ser2498= | |
| XM_006718845.1:c.3450T>C (ATM) | XP_006718908.1:p.Ser1150= | |
| XM_011542840.1:c.7494T>C (ATM) | XP_011541142.1:p.Ser2498= | |
| XM_011542841.1:c.7494T>C (ATM) | XP_011541143.1:p.Ser2498= | |
| XM_011542842.1:c.7329T>C (ATM) | XP_011541144.1:p.Ser2443= | |
| XM_011542843.1:c.7494T>C (ATM) | XP_011541145.1:p.Ser2498= | |
| XM_011542844.1:c.6450T>C (ATM) | XP_011541146.1:p.Ser2150= | |
| XM_011542845.1:c.6186T>C (ATM) | XP_011541147.1:p.Ser2062= | |
| XM_011542847.1:c.2565T>C (ATM) | XP_011541149.1:p.Ser855= | |
| NM_001330368.1:c.641-21329A>G (C11orf65) | NP_001317297.1:n.641-21329A>G | |
| NM_001351110.1:c.*38+4820A>G (C11orf65) | NP_001338039.1:n.*38+4820A>G | |
| NM_001351834.1:c.7494T>C (ATM) | NP_001338763.1:p.Ser2498= | |
| XM_005271562.5:c.7494T>C (ATM) | XP_005271619.2:p.Ser2498= | |
| XM_006718843.4:c.7494T>C (ATM) | XP_006718906.1:p.Ser2498= | |
| XM_006718845.2:c.3450T>C (ATM) | XP_006718908.1:p.Ser1150= | |
| XM_011542840.3:c.7494T>C (ATM) | XP_011541142.1:p.Ser2498= | |
| XM_011542842.3:c.7329T>C (ATM) | XP_011541144.1:p.Ser2443= | |
| XM_011542843.2:c.7494T>C (ATM) | XP_011541145.1:p.Ser2498= | |
| XM_011542844.3:c.6450T>C (ATM) | XP_011541146.1:p.Ser2150= | |
| XM_011542845.2:c.6186T>C (ATM) | XP_011541147.1:p.Ser2062= | |
| XM_017017789.2:c.7494T>C (ATM) | XP_016873278.1:p.Ser2498= | |
| XM_017017790.2:c.7494T>C (ATM) | XP_016873279.1:p.Ser2498= | |
| NM_001330368.2:c.641-21329A>G (C11orf65) | NP_001317297.1:n.641-21329A>G | |
| NM_001351110.2:c.*38+4820A>G (C11orf65) | NP_001338039.1:n.*38+4820A>G | |
| NM_001351834.2:c.7494T>C (ATM) | NP_001338763.1:p.Ser2498= | |
| NM_000051.4:c.7494T>C (ATM) MANE Select | NP_000042.3:p.Ser2498= |