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 |
|---|---|---|---|---|---|
| 3 | g.122283828T>A | CA354157781 | CASR | c.1643T>A (p.Phe548Tyr) c.1904T>A (p.Phe635Tyr) c.1874T>A (p.Phe625Tyr) c.1391T>A (p.Phe464Tyr) c.1286T>A (p.Phe429Tyr) | |
| 3 | g.122283828T>C | CA354157785 | CASR | c.1643T>C (p.Phe548Ser) c.1904T>C (p.Phe635Ser) c.1874T>C (p.Phe625Ser) c.1391T>C (p.Phe464Ser) c.1286T>C (p.Phe429Ser) | |
| 3 | g.122283828T>G | CA354157783 | CASR | c.1643T>G (p.Phe548Cys) c.1904T>G (p.Phe635Cys) c.1874T>G (p.Phe625Cys) c.1391T>G (p.Phe464Cys) c.1286T>G (p.Phe429Cys) | |
| 3 | g.122283829C>A | CA354157786 | CASR | c.1644C>A (p.Phe548Leu) c.1905C>A (p.Phe635Leu) c.1875C>A (p.Phe625Leu) c.1392C>A (p.Phe464Leu) c.1287C>A (p.Phe429Leu) | |
| 3 | g.122283829C= | CA1397871065 | CASR | c.1644C= (p.Phe548=) c.1905C= (p.Phe635=) c.1875C= (p.Phe625=) c.1392C= (p.Phe464=) c.1287C= (p.Phe429=) | |
| 3 | g.122283829C>G | CA354157788 | CASR | c.1644C>G (p.Phe548Leu) c.1905C>G (p.Phe635Leu) c.1875C>G (p.Phe625Leu) c.1392C>G (p.Phe464Leu) c.1287C>G (p.Phe429Leu) | |
| 3 | g.122283829C>T | CA2569755 | CASR | c.1644C>T (p.Phe548=) c.1905C>T (p.Phe635=) c.1875C>T (p.Phe625=) c.1392C>T (p.Phe464=) c.1287C>T (p.Phe429=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 3 | g.122283830C>A | CA354157792 | CASR | c.1645C>A (p.Leu549Met) c.1906C>A (p.Leu636Met) c.1876C>A (p.Leu626Met) c.1393C>A (p.Leu465Met) c.1288C>A (p.Leu430Met) | ClinVar dbSNP gnomAD v4 |
| 3 | g.122283830C>G | CA354157793 | CASR | c.1645C>G (p.Leu549Val) c.1906C>G (p.Leu636Val) c.1876C>G (p.Leu626Val) c.1393C>G (p.Leu465Val) c.1288C>G (p.Leu430Val) | |
| 3 | g.122283830C>T | CA435251921 | CASR | c.1645C>T (p.Leu549=) c.1906C>T (p.Leu636=) c.1876C>T (p.Leu626=) c.1393C>T (p.Leu465=) c.1288C>T (p.Leu430=) | |
| 3 | g.122283831T>A | CA354157799 | CASR | c.1646T>A (p.Leu549Gln) c.1907T>A (p.Leu636Gln) c.1877T>A (p.Leu626Gln) c.1394T>A (p.Leu465Gln) c.1289T>A (p.Leu430Gln) | |
| 3 | g.122283831T>C | CA354157798 | CASR | c.1646T>C (p.Leu549Pro) c.1907T>C (p.Leu636Pro) c.1877T>C (p.Leu626Pro) c.1394T>C (p.Leu465Pro) c.1289T>C (p.Leu430Pro) | |
| 3 | g.122283831T>G | CA354157796 | CASR | c.1646T>G (p.Leu549Arg) c.1907T>G (p.Leu636Arg) c.1877T>G (p.Leu626Arg) c.1394T>G (p.Leu465Arg) c.1289T>G (p.Leu430Arg) | |
| 3 | g.122283832G>A | CA435251924 | CASR | c.1647G>A (p.Leu549=) c.1908G>A (p.Leu636=) c.1878G>A (p.Leu626=) c.1395G>A (p.Leu465=) c.1290G>A (p.Leu430=) | ClinVar |
| 3 | g.122283832G>C | CA435251922 | CASR | c.1647G>C (p.Leu549=) c.1908G>C (p.Leu636=) c.1878G>C (p.Leu626=) c.1395G>C (p.Leu465=) c.1290G>C (p.Leu430=) | |
| 3 | g.122283832G>T | CA435251923 | CASR | c.1647G>T (p.Leu549=) c.1908G>T (p.Leu636=) c.1878G>T (p.Leu626=) c.1395G>T (p.Leu465=) c.1290G>T (p.Leu430=) | |
| 3 | g.122283833A>C | CA354157802 | CASR | c.1648A>C (p.Thr550Pro) c.1909A>C (p.Thr637Pro) c.1879A>C (p.Thr627Pro) c.1396A>C (p.Thr466Pro) c.1291A>C (p.Thr431Pro) | |
| 3 | g.122283833A>G | CA354157803 | CASR | c.1648A>G (p.Thr550Ala) c.1909A>G (p.Thr637Ala) c.1879A>G (p.Thr627Ala) c.1396A>G (p.Thr466Ala) c.1291A>G (p.Thr431Ala) | ClinVar |
| 3 | g.122283833A>T | CA354157805 | CASR | c.1648A>T (p.Thr550Ser) c.1909A>T (p.Thr637Ser) c.1879A>T (p.Thr627Ser) c.1396A>T (p.Thr466Ser) c.1291A>T (p.Thr431Ser) | |
| 3 | g.122283834C>A | CA354157807 | CASR | c.1649C>A (p.Thr550Lys) c.1910C>A (p.Thr637Lys) c.1880C>A (p.Thr627Lys) c.1397C>A (p.Thr466Lys) c.1292C>A (p.Thr431Lys) | ClinVar dbSNP |
| 3 | g.122283834C= | CA1397871067 | CASR | c.1649C= (p.Thr550=) c.1910C= (p.Thr637=) c.1880C= (p.Thr627=) c.1397C= (p.Thr466=) c.1292C= (p.Thr431=) | |
| 3 | g.122283834C>G | CA354157809 | CASR | c.1649C>G (p.Thr550Arg) c.1910C>G (p.Thr637Arg) c.1880C>G (p.Thr627Arg) c.1397C>G (p.Thr466Arg) c.1292C>G (p.Thr431Arg) | |
| 3 | g.122283834C>T | CA354157811 | CASR | c.1649C>T (p.Thr550Ile) c.1910C>T (p.Thr637Ile) c.1880C>T (p.Thr627Ile) c.1397C>T (p.Thr466Ile) c.1292C>T (p.Thr431Ile) | ClinVar dbSNP |
| 3 | g.122283835A= | CA1397871071 | CASR | c.1650A= (p.Thr550=) c.1911A= (p.Thr637=) c.1881A= (p.Thr627=) c.1398A= (p.Thr466=) c.1293A= (p.Thr431=) | |
| 3 | g.122283835A>C | CA435251926 | CASR | c.1650A>C (p.Thr550=) c.1911A>C (p.Thr637=) c.1881A>C (p.Thr627=) c.1398A>C (p.Thr466=) c.1293A>C (p.Thr431=) | |
| 3 | g.122283835A>G | CA435251927 | CASR | c.1650A>G (p.Thr550=) c.1911A>G (p.Thr637=) c.1881A>G (p.Thr627=) c.1398A>G (p.Thr466=) c.1293A>G (p.Thr431=) | |
| 3 | g.122283835A>T | CA435251928 | CASR | c.1650A>T (p.Thr550=) c.1911A>T (p.Thr637=) c.1881A>T (p.Thr627=) c.1398A>T (p.Thr466=) c.1293A>T (p.Thr431=) | dbSNP |
| 3 | g.122283836G>A | CA354157814 | CASR | c.1651G>A (p.Ala551Thr) c.1912G>A (p.Ala638Thr) c.1882G>A (p.Ala628Thr) c.1399G>A (p.Ala467Thr) c.1294G>A (p.Ala432Thr) | |
| 3 | g.122283836G>C | CA354157818 | CASR | c.1651G>C (p.Ala551Pro) c.1912G>C (p.Ala638Pro) c.1882G>C (p.Ala628Pro) c.1399G>C (p.Ala467Pro) c.1294G>C (p.Ala432Pro) | |
| 3 | g.122283836G>T | CA354157815 | CASR | c.1651G>T (p.Ala551Ser) c.1912G>T (p.Ala638Ser) c.1882G>T (p.Ala628Ser) c.1399G>T (p.Ala467Ser) c.1294G>T (p.Ala432Ser) | |
| 3 | g.122283836_122283837delinsGC | CA1397871073 | CASR | c.1651_1652delinsGC (p.Ala551=) c.1912_1913delinsGC (p.Ala638=) c.1882_1883delinsGC (p.Ala628=) c.1399_1400delinsGC (p.Ala467=) c.1294_1295delinsGC (p.Ala432=) | |
| 3 | g.122283837C>A | CA354157821 | CASR | c.1652C>A (p.Ala551Asp) c.1913C>A (p.Ala638Asp) c.1883C>A (p.Ala628Asp) c.1400C>A (p.Ala467Asp) c.1295C>A (p.Ala432Asp) | |
| 3 | g.122283837C>G | CA354157822 | CASR | c.1652C>G (p.Ala551Gly) c.1913C>G (p.Ala638Gly) c.1883C>G (p.Ala628Gly) c.1400C>G (p.Ala467Gly) c.1295C>G (p.Ala432Gly) | |
| 3 | g.122283837C>T | CA354157825 | CASR | c.1652C>T (p.Ala551Val) c.1913C>T (p.Ala638Val) c.1883C>T (p.Ala628Val) c.1400C>T (p.Ala467Val) c.1295C>T (p.Ala432Val) | gnomAD v4 |
| 3 | g.122283838del | CA213574 | CASR | c.1653del (p.Phe552LeufsTer?) c.1914del (p.Phe639LeufsTer?) c.1884del (p.Phe629LeufsTer?) c.1401del (p.Phe468LeufsTer?) c.1296del (p.Phe433LeufsTer?) | ClinVar dbSNP |
| 3 | g.122283838C>A | CA2569756 | CASR | c.1653C>A (p.Ala551=) c.1914C>A (p.Ala638=) c.1884C>A (p.Ala628=) c.1401C>A (p.Ala467=) c.1296C>A (p.Ala432=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.122283838C= | CA1397871078 | CASR | c.1653C= (p.Ala551=) c.1914C= (p.Ala638=) c.1884C= (p.Ala628=) c.1401C= (p.Ala467=) c.1296C= (p.Ala432=) | |
| 3 | g.122283838C>G | CA435251932 | CASR | c.1653C>G (p.Ala551=) c.1914C>G (p.Ala638=) c.1884C>G (p.Ala628=) c.1401C>G (p.Ala467=) c.1296C>G (p.Ala432=) | |
| 3 | g.122283838C>T | CA435251933 | CASR | c.1653C>T (p.Ala551=) c.1914C>T (p.Ala638=) c.1884C>T (p.Ala628=) c.1401C>T (p.Ala467=) c.1296C>T (p.Ala432=) | ClinVar |
| 3 | g.122283839T>A | CA354157830 | CASR | c.1654T>A (p.Phe552Ile) c.1915T>A (p.Phe639Ile) c.1885T>A (p.Phe629Ile) c.1402T>A (p.Phe468Ile) c.1297T>A (p.Phe433Ile) | |
| 3 | g.122283839T>C | CA354157832 | CASR | c.1654T>C (p.Phe552Leu) c.1915T>C (p.Phe639Leu) c.1885T>C (p.Phe629Leu) c.1402T>C (p.Phe468Leu) c.1297T>C (p.Phe433Leu) | |
| 3 | g.122283839T>G | CA354157834 | CASR | c.1654T>G (p.Phe552Val) c.1915T>G (p.Phe639Val) c.1885T>G (p.Phe629Val) c.1402T>G (p.Phe468Val) c.1297T>G (p.Phe433Val) | |
| 3 | g.122283840T>A | CA354157836 | CASR | c.1655T>A (p.Phe552Tyr) c.1916T>A (p.Phe639Tyr) c.1886T>A (p.Phe629Tyr) c.1403T>A (p.Phe468Tyr) c.1298T>A (p.Phe433Tyr) | |
| 3 | g.122283840T>C | CA354157838 | CASR | c.1655T>C (p.Phe552Ser) c.1916T>C (p.Phe639Ser) c.1886T>C (p.Phe629Ser) c.1403T>C (p.Phe468Ser) c.1298T>C (p.Phe433Ser) | gnomAD v4 |
| 3 | g.122283840T>G | CA354157840 | CASR | c.1655T>G (p.Phe552Cys) c.1916T>G (p.Phe639Cys) c.1886T>G (p.Phe629Cys) c.1403T>G (p.Phe468Cys) c.1298T>G (p.Phe433Cys) | |
| 3 | g.122283841T>A | CA354157843 | CASR | c.1656T>A (p.Phe552Leu) c.1917T>A (p.Phe639Leu) c.1887T>A (p.Phe629Leu) c.1404T>A (p.Phe468Leu) c.1299T>A (p.Phe433Leu) | |
| 3 | g.122283841T>C | CA2569757 | CASR | c.1656T>C (p.Phe552=) c.1917T>C (p.Phe639=) c.1887T>C (p.Phe629=) c.1404T>C (p.Phe468=) c.1299T>C (p.Phe433=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.122283841T>G | CA354157845 | CASR | c.1656T>G (p.Phe552Leu) c.1917T>G (p.Phe639Leu) c.1887T>G (p.Phe629Leu) c.1404T>G (p.Phe468Leu) c.1299T>G (p.Phe433Leu) | |
| 3 | g.122283841T= | CA1397871081 | CASR | c.1656T= (p.Phe552=) c.1917T= (p.Phe639=) c.1887T= (p.Phe629=) c.1404T= (p.Phe468=) c.1299T= (p.Phe433=) | |
| 3 | g.122283842G>A | CA354157847 | CASR | c.1657G>A (p.Val553Met) c.1918G>A (p.Val640Met) c.1888G>A (p.Val630Met) c.1405G>A (p.Val469Met) c.1300G>A (p.Val434Met) | ClinVar dbSNP gnomAD v4 |