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 |
|---|---|---|---|---|---|
| 1 | g.214657084G>A | CA423429477 | CENPF | c.8460G>A (p.Glu2820=) n.736G>A c.8637G>A (p.Glu2879=) n.408G>A c.7572G>A (p.Glu2524=) | gnomAD v4 |
| 1 | g.214657084G>C | CA344856816 | CENPF | c.8460G>C (p.Glu2820Asp) n.736G>C c.8637G>C (p.Glu2879Asp) n.408G>C c.7572G>C (p.Glu2524Asp) | |
| 1 | g.214657084G>T | CA344856817 | CENPF | c.8460G>T (p.Glu2820Asp) n.736G>T c.8637G>T (p.Glu2879Asp) n.408G>T c.7572G>T (p.Glu2524Asp) | |
| 1 | g.214657085A>C | CA344856818 | CENPF | c.8461A>C (p.Met2821Leu) n.737A>C c.8638A>C (p.Met2880Leu) n.409A>C c.7573A>C (p.Met2525Leu) | |
| 1 | g.214657085A>G | CA344856819 | CENPF | c.8461A>G (p.Met2821Val) n.737A>G c.8638A>G (p.Met2880Val) n.409A>G c.7573A>G (p.Met2525Val) | COSMIC |
| 1 | g.214657085A>T | CA344856820 | CENPF | c.8461A>T (p.Met2821Leu) n.737A>T c.8638A>T (p.Met2880Leu) n.409A>T c.7573A>T (p.Met2525Leu) | |
| 1 | g.214657086T>A | CA344856821 | CENPF | c.8462T>A (p.Met2821Lys) n.738T>A c.8639T>A (p.Met2880Lys) n.410T>A c.7574T>A (p.Met2525Lys) | |
| 1 | g.214657086T>C | CA344856822 | CENPF | c.8462T>C (p.Met2821Thr) n.738T>C c.8639T>C (p.Met2880Thr) n.410T>C c.7574T>C (p.Met2525Thr) | |
| 1 | g.214657086T>G | CA344856823 | CENPF | c.8462T>G (p.Met2821Arg) n.738T>G c.8639T>G (p.Met2880Arg) n.410T>G c.7574T>G (p.Met2525Arg) | |
| 1 | g.214657087G>A | CA344856824 | CENPF | c.8463G>A (p.Met2821Ile) n.739G>A c.8640G>A (p.Met2880Ile) n.411G>A c.7575G>A (p.Met2525Ile) | |
| 1 | g.214657087G>C | CA344856825 | CENPF | c.8463G>C (p.Met2821Ile) n.739G>C c.8640G>C (p.Met2880Ile) n.411G>C c.7575G>C (p.Met2525Ile) | |
| 1 | g.214657087G>T | CA344856826 | CENPF | c.8463G>T (p.Met2821Ile) n.739G>T c.8640G>T (p.Met2880Ile) n.411G>T c.7575G>T (p.Met2525Ile) | |
| 1 | g.214657088T>A | CA344856827 | CENPF | c.8464T>A (p.Leu2822Ile) n.740T>A c.8641T>A (p.Leu2881Ile) n.412T>A c.7576T>A (p.Leu2526Ile) | |
| 1 | g.214657088T>C | CA423429484 | CENPF | c.8464T>C (p.Leu2822=) n.740T>C c.8641T>C (p.Leu2881=) n.412T>C c.7576T>C (p.Leu2526=) | |
| 1 | g.214657088T>G | CA344856828 | CENPF | c.8464T>G (p.Leu2822Val) n.740T>G c.8641T>G (p.Leu2881Val) n.412T>G c.7576T>G (p.Leu2526Val) | |
| 1 | g.214657089T>A | CA344856831 | CENPF | c.8465T>A (p.Leu2822Ter) n.741T>A c.8642T>A (p.Leu2881Ter) n.413T>A c.7577T>A (p.Leu2526Ter) | |
| 1 | g.214657089T>C | CA344856830 | CENPF | c.8465T>C (p.Leu2822Ser) n.741T>C c.8642T>C (p.Leu2881Ser) n.413T>C c.7577T>C (p.Leu2526Ser) | dbSNP |
| 1 | g.214657089T>G | CA344856829 | CENPF | c.8465T>G (p.Leu2822Ter) n.741T>G c.8642T>G (p.Leu2881Ter) n.413T>G c.7577T>G (p.Leu2526Ter) | |
| 1 | g.214657089T= | CA2486377607 | CENPF | c.8465T= (p.Leu2822=) n.741T= c.8642T= (p.Leu2881=) n.413T= c.7577T= (p.Leu2526=) | |
| 1 | g.214657090A>C | CA344856832 | CENPF | c.8466A>C (p.Leu2822Phe) n.742A>C c.8643A>C (p.Leu2881Phe) n.414A>C c.7578A>C (p.Leu2526Phe) | |
| 1 | g.214657090A>G | CA423429489 | CENPF | c.8466A>G (p.Leu2822=) n.742A>G c.8643A>G (p.Leu2881=) n.414A>G c.7578A>G (p.Leu2526=) | gnomAD v4 |
| 1 | g.214657090A>T | CA344856833 | CENPF | c.8466A>T (p.Leu2822Phe) n.742A>T c.8643A>T (p.Leu2881Phe) n.414A>T c.7578A>T (p.Leu2526Phe) | |
| 1 | g.214657091G>A | CA344856834 | CENPF | c.8467G>A (p.Glu2823Lys) n.743G>A c.8644G>A (p.Glu2882Lys) n.415G>A c.7579G>A (p.Glu2527Lys) | |
| 1 | g.214657091G>C | CA344856835 | CENPF | c.8467G>C (p.Glu2823Gln) n.743G>C c.8644G>C (p.Glu2882Gln) n.415G>C c.7579G>C (p.Glu2527Gln) | |
| 1 | g.214657091G>T | CA344856836 | CENPF | c.8467G>T (p.Glu2823Ter) n.743G>T c.8644G>T (p.Glu2882Ter) n.415G>T c.7579G>T (p.Glu2527Ter) | |
| 1 | g.214657092A= | CA2486377608 | CENPF | c.8468A= (p.Glu2823=) n.744A= c.8645A= (p.Glu2882=) n.416A= c.7580A= (p.Glu2527=) | |
| 1 | g.214657092A>C | CA344856837 | CENPF | c.8468A>C (p.Glu2823Ala) n.744A>C c.8645A>C (p.Glu2882Ala) n.416A>C c.7580A>C (p.Glu2527Ala) | gnomAD v4 |
| 1 | g.214657092A>G | CA1391466 | CENPF | c.8468A>G (p.Glu2823Gly) n.744A>G c.8645A>G (p.Glu2882Gly) n.416A>G c.7580A>G (p.Glu2527Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.214657092A>T | CA344856838 | CENPF | c.8468A>T (p.Glu2823Val) n.744A>T c.8645A>T (p.Glu2882Val) n.416A>T c.7580A>T (p.Glu2527Val) | |
| 1 | g.214657093G>A | CA423429496 | CENPF | c.8469G>A (p.Glu2823=) n.745G>A c.8646G>A (p.Glu2882=) n.417G>A c.7581G>A (p.Glu2527=) | |
| 1 | g.214657093G>C | CA344856839 | CENPF | c.8469G>C (p.Glu2823Asp) n.745G>C c.8646G>C (p.Glu2882Asp) n.417G>C c.7581G>C (p.Glu2527Asp) | |
| 1 | g.214657093G>T | CA344856840 | CENPF | c.8469G>T (p.Glu2823Asp) n.745G>T c.8646G>T (p.Glu2882Asp) n.417G>T c.7581G>T (p.Glu2527Asp) | |
| 1 | g.214657094A= | CA1142064894 | CENPF | c.8470A= (p.Thr2824=) n.746A= c.8647A= (p.Thr2883=) n.418A= c.7582A= (p.Thr2528=) | |
| 1 | g.214657094A>C | CA344856841 | CENPF | c.8470A>C (p.Thr2824Pro) n.746A>C c.8647A>C (p.Thr2883Pro) n.418A>C c.7582A>C (p.Thr2528Pro) | |
| 1 | g.214657094A>G | CA37381015 | CENPF | c.8470A>G (p.Thr2824Ala) n.746A>G c.8647A>G (p.Thr2883Ala) n.418A>G c.7582A>G (p.Thr2528Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.214657094A>T | CA344856842 | CENPF | c.8470A>T (p.Thr2824Ser) n.746A>T c.8647A>T (p.Thr2883Ser) n.418A>T c.7582A>T (p.Thr2528Ser) | |
| 1 | g.214657095C>A | CA344856844 | CENPF | c.8471C>A (p.Thr2824Lys) n.747C>A c.8648C>A (p.Thr2883Lys) n.419C>A c.7583C>A (p.Thr2528Lys) | |
| 1 | g.214657095C>G | CA344856845 | CENPF | c.8471C>G (p.Thr2824Arg) n.747C>G c.8648C>G (p.Thr2883Arg) n.419C>G c.7583C>G (p.Thr2528Arg) | |
| 1 | g.214657095C>T | CA344856843 | CENPF | c.8471C>T (p.Thr2824Ile) n.747C>T c.8648C>T (p.Thr2883Ile) n.419C>T c.7583C>T (p.Thr2528Ile) | |
| 1 | g.214657096A>C | CA423429501 | CENPF | c.8472A>C (p.Thr2824=) n.748A>C c.8649A>C (p.Thr2883=) n.420A>C c.7584A>C (p.Thr2528=) | |
| 1 | g.214657096A>G | CA423429502 | CENPF | c.8472A>G (p.Thr2824=) n.748A>G c.8649A>G (p.Thr2883=) n.420A>G c.7584A>G (p.Thr2528=) | |
| 1 | g.214657096A>T | CA423429503 | CENPF | c.8472A>T (p.Thr2824=) n.748A>T c.8649A>T (p.Thr2883=) n.420A>T c.7584A>T (p.Thr2528=) | |
| 1 | g.214657097C>A | CA344856848 | CENPF | c.8473C>A (p.Gln2825Lys) n.749C>A c.8650C>A (p.Gln2884Lys) n.421C>A c.7585C>A (p.Gln2529Lys) | |
| 1 | g.214657097C>G | CA344856846 | CENPF | c.8473C>G (p.Gln2825Glu) n.749C>G c.8650C>G (p.Gln2884Glu) n.421C>G c.7585C>G (p.Gln2529Glu) | |
| 1 | g.214657097C>T | CA344856847 | CENPF | c.8473C>T (p.Gln2825Ter) n.749C>T c.8650C>T (p.Gln2884Ter) n.421C>T c.7585C>T (p.Gln2529Ter) | |
| 1 | g.214657098A= | CA2486377614 | CENPF | c.8474A= (p.Gln2825=) n.750A= c.8651A= (p.Gln2884=) n.422A= c.7586A= (p.Gln2529=) | |
| 1 | g.214657098A>C | CA344856849 | CENPF | c.8474A>C (p.Gln2825Pro) n.750A>C c.8651A>C (p.Gln2884Pro) n.422A>C c.7586A>C (p.Gln2529Pro) | |
| 1 | g.214657098A>G | CA344856850 | CENPF | c.8474A>G (p.Gln2825Arg) n.750A>G c.8651A>G (p.Gln2884Arg) n.422A>G c.7586A>G (p.Gln2529Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.214657098A>T | CA344856851 | CENPF | c.8474A>T (p.Gln2825Leu) n.750A>T c.8651A>T (p.Gln2884Leu) n.422A>T c.7586A>T (p.Gln2529Leu) | |
| 1 | g.214657099A= | CA2486377616 | CENPF | c.8475A= (p.Gln2825=) n.751A= c.8652A= (p.Gln2884=) n.423A= c.7587A= (p.Gln2529=) |