UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66435071_66435118del | CA645570529 | MAP2K1 | c.59_106del (p.Leu20_Lys35del) c.125_172del (p.Leu42_Lys57del) n.561_608del n.636_683del | COSMIC |
| 15 | g.66435071_66435074delinsTTGA | CA2184071720 | MAP2K1 | c.59_62delinsTTGA (p.Leu20=) c.125_128delinsTTGA (p.Leu42=) n.561_564delinsTTGA n.636_639delinsTTGA | |
| 15 | g.66435075_66435077del | CA658656490 | MAP2K1 | c.63_65del (p.Asp21del) c.129_131del (p.Asp43del) n.565_567del n.640_642del | ClinVar dbSNP |
| 15 | g.66435073G>A | CA392929056 | MAP2K1 | c.61G>A (p.Asp21Asn) c.127G>A (p.Asp43Asn) n.563G>A n.638G>A | dbSNP |
| 15 | g.66435073G>C | CA392929054 | MAP2K1 | c.61G>C (p.Asp21His) c.127G>C (p.Asp43His) n.563G>C n.638G>C | dbSNP |
| 15 | g.66435073G>T | CA392929053 | MAP2K1 | c.61G>T (p.Asp21Tyr) c.127G>T (p.Asp43Tyr) n.563G>T n.638G>T | dbSNP |
| 15 | g.66435074A>C | CA392929058 | MAP2K1 | c.62A>C (p.Asp21Ala) c.128A>C (p.Asp43Ala) n.564A>C n.639A>C | |
| 15 | g.66435074A>G | CA392929060 | MAP2K1 | c.62A>G (p.Asp21Gly) c.128A>G (p.Asp43Gly) n.564A>G n.639A>G | dbSNP |
| 15 | g.66435074A>T | CA392929062 | MAP2K1 | c.62A>T (p.Asp21Val) c.128A>T (p.Asp43Val) n.564A>T n.639A>T | dbSNP |
| 15 | g.66435075T>A | CA392929064 | MAP2K1 | c.63T>A (p.Asp21Glu) c.129T>A (p.Asp43Glu) n.565T>A n.640T>A | |
| 15 | g.66435075T>C | CA490855910 | MAP2K1 | c.63T>C (p.Asp21=) c.129T>C (p.Asp43=) n.565T>C n.640T>C | |
| 15 | g.66435075T>G | CA392929065 | MAP2K1 | c.63T>G (p.Asp21Glu) c.129T>G (p.Asp43Glu) n.565T>G n.640T>G | |
| 15 | g.66435076_66435108del | CA2573151054 | MAP2K1 | c.64_96del (p.Glu22_Leu32del) c.130_162del (p.Glu44_Leu54del) n.566_598del n.641_673del | ClinVar dbSNP |
| 15 | g.66435076G>A | CA392929068 | MAP2K1 | c.64G>A (p.Glu22Lys) c.130G>A (p.Glu44Lys) n.566G>A n.641G>A | dbSNP |
| 15 | g.66435076G>C | CA392929069 | MAP2K1 | c.64G>C (p.Glu22Gln) c.130G>C (p.Glu44Gln) n.566G>C n.641G>C | dbSNP |
| 15 | g.66435076G>T | CA392929071 | MAP2K1 | c.64G>T (p.Glu22Ter) c.130G>T (p.Glu44Ter) n.566G>T n.641G>T | dbSNP gnomAD v4 |
| 15 | g.66435077A= | CA2184071723 | MAP2K1 | c.65A= (p.Glu22=) c.131A= (p.Glu44=) n.567A= n.642A= | |
| 15 | g.66435077A>C | CA392929073 | MAP2K1 | c.65A>C (p.Glu22Ala) c.131A>C (p.Glu44Ala) n.567A>C n.642A>C | |
| 15 | g.66435077A>G | CA392929075 | MAP2K1 | c.65A>G (p.Glu22Gly) c.131A>G (p.Glu44Gly) n.567A>G n.642A>G | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.66435077A>T | CA392929077 | MAP2K1 | c.65A>T (p.Glu22Val) c.131A>T (p.Glu44Val) n.567A>T n.642A>T | dbSNP |
| 15 | g.66435078G>A | CA490855911 | MAP2K1 | c.66G>A (p.Glu22=) c.132G>A (p.Glu44=) n.568G>A n.643G>A | dbSNP gnomAD v4 |
| 15 | g.66435078G>C | CA392929079 | MAP2K1 | c.66G>C (p.Glu22Asp) c.132G>C (p.Glu44Asp) n.568G>C n.643G>C | dbSNP |
| 15 | g.66435078G= | CA2184071724 | MAP2K1 | c.66G= (p.Glu22=) c.132G= (p.Glu44=) n.568G= n.643G= | |
| 15 | g.66435078G>T | CA392929080 | MAP2K1 | c.66G>T (p.Glu22Asp) c.132G>T (p.Glu44Asp) n.568G>T n.643G>T | |
| 15 | g.66435079C>A | CA392929086 | MAP2K1 | c.67C>A (p.Gln23Lys) c.133C>A (p.Gln45Lys) n.569C>A n.644C>A | |
| 15 | g.66435079C>G | CA392929083 | MAP2K1 | c.67C>G (p.Gln23Glu) c.133C>G (p.Gln45Glu) n.569C>G n.644C>G | dbSNP |
| 15 | g.66435079C>T | CA392929084 | MAP2K1 | c.67C>T (p.Gln23Ter) c.133C>T (p.Gln45Ter) n.569C>T n.644C>T | dbSNP |
| 15 | g.66435080A>C | CA392929087 | MAP2K1 | c.68A>C (p.Gln23Pro) c.134A>C (p.Gln45Pro) n.570A>C n.645A>C | |
| 15 | g.66435080A>G | CA392929089 | MAP2K1 | c.68A>G (p.Gln23Arg) c.134A>G (p.Gln45Arg) n.570A>G n.645A>G | |
| 15 | g.66435080A>T | CA392929091 | MAP2K1 | c.68A>T (p.Gln23Leu) c.134A>T (p.Gln45Leu) n.570A>T n.645A>T | dbSNP |
| 15 | g.66435081G>A | CA490855912 | MAP2K1 | c.69G>A (p.Gln23=) c.135G>A (p.Gln45=) n.571G>A n.646G>A | dbSNP gnomAD v4 |
| 15 | g.66435081G>C | CA392929092 | MAP2K1 | c.69G>C (p.Gln23His) c.135G>C (p.Gln45His) n.571G>C n.646G>C | dbSNP |
| 15 | g.66435081G= | CA2184071725 | MAP2K1 | c.69G= (p.Gln23=) c.135G= (p.Gln45=) n.571G= n.646G= | |
| 15 | g.66435081G>T | CA392929095 | MAP2K1 | c.69G>T (p.Gln23His) c.135G>T (p.Gln45His) n.571G>T n.646G>T | ClinVar dbSNP gnomAD v4 |
| 15 | g.66435082C>A | CA392929097 | MAP2K1 | c.70C>A (p.Gln24Lys) c.136C>A (p.Gln46Lys) n.572C>A n.647C>A | |
| 15 | g.66435082C>G | CA392929098 | MAP2K1 | c.70C>G (p.Gln24Glu) c.136C>G (p.Gln46Glu) n.572C>G n.647C>G | dbSNP |
| 15 | g.66435082C>T | CA392929101 | MAP2K1 | c.70C>T (p.Gln24Ter) c.136C>T (p.Gln46Ter) n.572C>T n.647C>T | dbSNP |
| 15 | g.66435083A= | CA2184071726 | MAP2K1 | c.71A= (p.Gln24=) c.137A= (p.Gln46=) n.573A= n.648A= | |
| 15 | g.66435083A>C | CA392929103 | MAP2K1 | c.71A>C (p.Gln24Pro) c.137A>C (p.Gln46Pro) n.573A>C n.648A>C | |
| 15 | g.66435083A>G | CA392929104 | MAP2K1 | c.71A>G (p.Gln24Arg) c.137A>G (p.Gln46Arg) n.573A>G n.648A>G | |
| 15 | g.66435083A>T | CA392929105 | MAP2K1 | c.71A>T (p.Gln24Leu) c.137A>T (p.Gln46Leu) n.573A>T n.648A>T | ClinVar dbSNP |
| 15 | g.66435084del | CA2697549135 | MAP2K1 | c.72del (p.Gln24HisfsTer18) c.138del (p.Gln46HisfsTer18) n.574del n.649del | ClinVar |
| 15 | g.66435084G>A | CA490855913 | MAP2K1 | c.72G>A (p.Gln24=) c.138G>A (p.Gln46=) n.574G>A n.649G>A | dbSNP |
| 15 | g.66435084G>C | CA392929117 | MAP2K1 | c.72G>C (p.Gln24His) c.138G>C (p.Gln46His) n.574G>C n.649G>C | dbSNP |
| 15 | g.66435084G>T | CA392929118 | MAP2K1 | c.72G>T (p.Gln24His) c.138G>T (p.Gln46His) n.574G>T n.649G>T | |
| 15 | g.66435085C>A | CA490855914 | MAP2K1 | c.73C>A (p.Arg25=) c.139C>A (p.Arg47=) n.575C>A n.650C>A | ClinVar dbSNP |
| 15 | g.66435085C= | CA2184071727 | MAP2K1 | c.73C= (p.Arg25=) c.139C= (p.Arg47=) n.575C= n.650C= | |
| 15 | g.66435085C>G | CA392929120 | MAP2K1 | c.73C>G (p.Arg25Gly) c.139C>G (p.Arg47Gly) n.575C>G n.650C>G | dbSNP |
| 15 | g.66435085C>T | CA271640690 | MAP2K1 | c.73C>T (p.Arg25Ter) c.139C>T (p.Arg47Ter) n.575C>T n.650C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.66435086G>A | CA392929123 | MAP2K1 | c.74G>A (p.Arg25Gln) c.140G>A (p.Arg47Gln) n.576G>A n.651G>A | ClinVar dbSNP gnomAD v4 COSMIC |