WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.36234106G>A | CA340501 | CLTA,GNE | c.889C>T (p.Arg297Trp) c.619C>T (p.Arg207Trp) c.796C>T (p.Arg266Trp) c.486-29092G>A (n.486-29092G>A) c.466C>T (p.Arg156Trp) c.781C>T (p.Arg261Trp) c.736C>T (p.Arg246Trp) c.643C>T (p.Arg215Trp) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC |
| 9 | g.36234106G>C | CA373430858 | CLTA,GNE | c.889C>G (p.Arg297Gly) c.619C>G (p.Arg207Gly) c.796C>G (p.Arg266Gly) c.486-29092G>C (n.486-29092G>C) c.466C>G (p.Arg156Gly) c.781C>G (p.Arg261Gly) c.736C>G (p.Arg246Gly) c.643C>G (p.Arg215Gly) | |
| 9 | g.36234106G= | CA1846355728 | CLTA,GNE | c.889C= (p.Arg297=) c.619C= (p.Arg207=) c.796C= (p.Arg266=) c.486-29092G= (n.486-29092G=) c.466C= (p.Arg156=) c.781C= (p.Arg261=) c.736C= (p.Arg246=) c.643C= (p.Arg215=) | |
| 9 | g.36234106G>T | CA464496080 | CLTA,GNE | c.889C>A (p.Arg297=) c.619C>A (p.Arg207=) c.796C>A (p.Arg266=) c.486-29092G>T (n.486-29092G>T) c.466C>A (p.Arg156=) c.781C>A (p.Arg261=) c.736C>A (p.Arg246=) c.643C>A (p.Arg215=) | |
| 9 | g.36234107C>A | CA373430859 | CLTA,GNE | c.888G>T (p.Met296Ile) c.618G>T (p.Met206Ile) c.795G>T (p.Met265Ile) c.486-29091C>A (n.486-29091C>A) c.465G>T (p.Met155Ile) c.780G>T (p.Met260Ile) c.735G>T (p.Met245Ile) c.642G>T (p.Met214Ile) | ClinVar dbSNP gnomAD v4 |
| 9 | g.36234107C= | CA1846355734 | CLTA,GNE | c.888G= (p.Met296=) c.618G= (p.Met206=) c.795G= (p.Met265=) c.486-29091C= (n.486-29091C=) c.465G= (p.Met155=) c.780G= (p.Met260=) c.735G= (p.Met245=) c.642G= (p.Met214=) | |
| 9 | g.36234107C>G | CA373430860 | CLTA,GNE | c.888G>C (p.Met296Ile) c.618G>C (p.Met206Ile) c.795G>C (p.Met265Ile) c.486-29091C>G (n.486-29091C>G) c.465G>C (p.Met155Ile) c.780G>C (p.Met260Ile) c.735G>C (p.Met245Ile) c.642G>C (p.Met214Ile) | |
| 9 | g.36234107C>T | CA373430861 | CLTA,GNE | c.888G>A (p.Met296Ile) c.618G>A (p.Met206Ile) c.795G>A (p.Met265Ile) c.486-29091C>T (n.486-29091C>T) c.465G>A (p.Met155Ile) c.780G>A (p.Met260Ile) c.735G>A (p.Met245Ile) c.642G>A (p.Met214Ile) | dbSNP gnomAD v4 |
| 9 | g.36234108A>C | CA373430862 | CLTA,GNE | c.887T>G (p.Met296Arg) c.617T>G (p.Met206Arg) c.794T>G (p.Met265Arg) c.486-29090A>C (n.486-29090A>C) c.464T>G (p.Met155Arg) c.779T>G (p.Met260Arg) c.734T>G (p.Met245Arg) c.641T>G (p.Met214Arg) | |
| 9 | g.36234108A>G | CA373430863 | CLTA,GNE | c.887T>C (p.Met296Thr) c.617T>C (p.Met206Thr) c.794T>C (p.Met265Thr) c.486-29090A>G (n.486-29090A>G) c.464T>C (p.Met155Thr) c.779T>C (p.Met260Thr) c.734T>C (p.Met245Thr) c.641T>C (p.Met214Thr) | ClinVar dbSNP gnomAD v4 |
| 9 | g.36234108A>T | CA373430864 | CLTA,GNE | c.887T>A (p.Met296Lys) c.617T>A (p.Met206Lys) c.794T>A (p.Met265Lys) c.486-29090A>T (n.486-29090A>T) c.464T>A (p.Met155Lys) c.779T>A (p.Met260Lys) c.734T>A (p.Met245Lys) c.641T>A (p.Met214Lys) | |
| 9 | g.36234109T>A | CA373430865 | CLTA,GNE | c.886A>T (p.Met296Leu) c.616A>T (p.Met206Leu) c.793A>T (p.Met265Leu) c.486-29089T>A (n.486-29089T>A) c.463A>T (p.Met155Leu) c.778A>T (p.Met260Leu) c.733A>T (p.Met245Leu) c.640A>T (p.Met214Leu) | |
| 9 | g.36234109T>C | CA373430866 | CLTA,GNE | c.886A>G (p.Met296Val) c.616A>G (p.Met206Val) c.793A>G (p.Met265Val) c.486-29089T>C (n.486-29089T>C) c.463A>G (p.Met155Val) c.778A>G (p.Met260Val) c.733A>G (p.Met245Val) c.640A>G (p.Met214Val) | |
| 9 | g.36234109T>G | CA373430867 | CLTA,GNE | c.886A>C (p.Met296Leu) c.616A>C (p.Met206Leu) c.793A>C (p.Met265Leu) c.486-29089T>G (n.486-29089T>G) c.463A>C (p.Met155Leu) c.778A>C (p.Met260Leu) c.733A>C (p.Met245Leu) c.640A>C (p.Met214Leu) | |
| 9 | g.36234110C>A | CA464496083 | CLTA,GNE | c.885G>T (p.Val295=) c.615G>T (p.Val205=) c.792G>T (p.Val264=) c.486-29088C>A (n.486-29088C>A) c.462G>T (p.Val154=) c.777G>T (p.Val259=) c.732G>T (p.Val244=) c.639G>T (p.Val213=) | |
| 9 | g.36234110C>G | CA464496081 | CLTA,GNE | c.885G>C (p.Val295=) c.615G>C (p.Val205=) c.792G>C (p.Val264=) c.486-29088C>G (n.486-29088C>G) c.462G>C (p.Val154=) c.777G>C (p.Val259=) c.732G>C (p.Val244=) c.639G>C (p.Val213=) | |
| 9 | g.36234110C>T | CA464496082 | CLTA,GNE | c.885G>A (p.Val295=) c.615G>A (p.Val205=) c.792G>A (p.Val264=) c.486-29088C>T (n.486-29088C>T) c.462G>A (p.Val154=) c.777G>A (p.Val259=) c.732G>A (p.Val244=) c.639G>A (p.Val213=) | |
| 9 | g.36234111A>C | CA373430868 | CLTA,GNE | c.884T>G (p.Val295Gly) c.614T>G (p.Val205Gly) c.791T>G (p.Val264Gly) c.486-29087A>C (n.486-29087A>C) c.461T>G (p.Val154Gly) c.776T>G (p.Val259Gly) c.731T>G (p.Val244Gly) c.638T>G (p.Val213Gly) | |
| 9 | g.36234111A>G | CA373430869 | CLTA,GNE | c.884T>C (p.Val295Ala) c.614T>C (p.Val205Ala) c.791T>C (p.Val264Ala) c.486-29087A>G (n.486-29087A>G) c.461T>C (p.Val154Ala) c.776T>C (p.Val259Ala) c.731T>C (p.Val244Ala) c.638T>C (p.Val213Ala) | |
| 9 | g.36234111A>T | CA373430870 | CLTA,GNE | c.884T>A (p.Val295Glu) c.614T>A (p.Val205Glu) c.791T>A (p.Val264Glu) c.486-29087A>T (n.486-29087A>T) c.461T>A (p.Val154Glu) c.776T>A (p.Val259Glu) c.731T>A (p.Val244Glu) c.638T>A (p.Val213Glu) | |
| 9 | g.36234112C>A | CA373430872 | CLTA,GNE | c.883G>T (p.Val295Leu) c.613G>T (p.Val205Leu) c.790G>T (p.Val264Leu) c.486-29086C>A (n.486-29086C>A) c.460G>T (p.Val154Leu) c.775G>T (p.Val259Leu) c.730G>T (p.Val244Leu) c.637G>T (p.Val213Leu) | |
| 9 | g.36234112C>G | CA373430873 | CLTA,GNE | c.883G>C (p.Val295Leu) c.613G>C (p.Val205Leu) c.790G>C (p.Val264Leu) c.486-29086C>G (n.486-29086C>G) c.460G>C (p.Val154Leu) c.775G>C (p.Val259Leu) c.730G>C (p.Val244Leu) c.637G>C (p.Val213Leu) | |
| 9 | g.36234112C>T | CA373430871 | CLTA,GNE | c.883G>A (p.Val295Met) c.613G>A (p.Val205Met) c.790G>A (p.Val264Met) c.486-29086C>T (n.486-29086C>T) c.460G>A (p.Val154Met) c.775G>A (p.Val259Met) c.730G>A (p.Val244Met) c.637G>A (p.Val213Met) | |
| 9 | g.36234113del | CA2689947396 | CLTA,GNE | c.882del (p.Val295Ter) c.612del (p.Val205Ter) c.789del (p.Val264Ter) c.486-29085del (n.486-29085del) c.459del (p.Val154Ter) c.774del (p.Val259Ter) c.729del (p.Val244Ter) c.636del (p.Val213Ter) | gnomAD v4 |
| 9 | g.36234113T>A | CA464496084 | CLTA,GNE | c.882A>T (p.Arg294=) c.612A>T (p.Arg204=) c.789A>T (p.Arg263=) c.486-29085T>A (n.486-29085T>A) c.459A>T (p.Arg153=) c.774A>T (p.Arg258=) c.729A>T (p.Arg243=) c.636A>T (p.Arg212=) | |
| 9 | g.36234113T>C | CA464496086 | CLTA,GNE | c.882A>G (p.Arg294=) c.612A>G (p.Arg204=) c.789A>G (p.Arg263=) c.486-29085T>C (n.486-29085T>C) c.459A>G (p.Arg153=) c.774A>G (p.Arg258=) c.729A>G (p.Arg243=) c.636A>G (p.Arg212=) | |
| 9 | g.36234113T>G | CA464496085 | CLTA,GNE | c.882A>C (p.Arg294=) c.612A>C (p.Arg204=) c.789A>C (p.Arg263=) c.486-29085T>G (n.486-29085T>G) c.459A>C (p.Arg153=) c.774A>C (p.Arg258=) c.729A>C (p.Arg243=) c.636A>C (p.Arg212=) | |
| 9 | g.36234114C>A | CA340505 | CLTA,GNE | c.881G>T (p.Arg294Leu) c.611G>T (p.Arg204Leu) c.788G>T (p.Arg263Leu) c.486-29084C>A (n.486-29084C>A) c.458G>T (p.Arg153Leu) c.773G>T (p.Arg258Leu) c.728G>T (p.Arg243Leu) c.635G>T (p.Arg212Leu) | ClinVar dbSNP |
| 9 | g.36234114C= | CA1846355748 | CLTA,GNE | c.881G= (p.Arg294=) c.611G= (p.Arg204=) c.788G= (p.Arg263=) c.486-29084C= (n.486-29084C=) c.458G= (p.Arg153=) c.773G= (p.Arg258=) c.728G= (p.Arg243=) c.635G= (p.Arg212=) | |
| 9 | g.36234114C>G | CA373430874 | CLTA,GNE | c.881G>C (p.Arg294Pro) c.611G>C (p.Arg204Pro) c.788G>C (p.Arg263Pro) c.486-29084C>G (n.486-29084C>G) c.458G>C (p.Arg153Pro) c.773G>C (p.Arg258Pro) c.728G>C (p.Arg243Pro) c.635G>C (p.Arg212Pro) | |
| 9 | g.36234114C>T | CA373430875 | CLTA,GNE | c.881G>A (p.Arg294Gln) c.611G>A (p.Arg204Gln) c.788G>A (p.Arg263Gln) c.486-29084C>T (n.486-29084C>T) c.458G>A (p.Arg153Gln) c.773G>A (p.Arg258Gln) c.728G>A (p.Arg243Gln) c.635G>A (p.Arg212Gln) | ClinVar COSMIC COSMIC COSMIC |
| 9 | g.36234115G>A | CA5056654 | CLTA,GNE | c.880C>T (p.Arg294Ter) c.610C>T (p.Arg204Ter) c.787C>T (p.Arg263Ter) c.486-29083G>A (n.486-29083G>A) c.457C>T (p.Arg153Ter) c.772C>T (p.Arg258Ter) c.727C>T (p.Arg243Ter) c.634C>T (p.Arg212Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.36234115G>C | CA373430876 | CLTA,GNE | c.880C>G (p.Arg294Gly) c.610C>G (p.Arg204Gly) c.787C>G (p.Arg263Gly) c.486-29083G>C (n.486-29083G>C) c.457C>G (p.Arg153Gly) c.772C>G (p.Arg258Gly) c.727C>G (p.Arg243Gly) c.634C>G (p.Arg212Gly) | |
| 9 | g.36234115G= | CA1846355758 | CLTA,GNE | c.880C= (p.Arg294=) c.610C= (p.Arg204=) c.787C= (p.Arg263=) c.486-29083G= (n.486-29083G=) c.457C= (p.Arg153=) c.772C= (p.Arg258=) c.727C= (p.Arg243=) c.634C= (p.Arg212=) | |
| 9 | g.36234115G>T | CA464496087 | CLTA,GNE | c.880C>A (p.Arg294=) c.610C>A (p.Arg204=) c.787C>A (p.Arg263=) c.486-29083G>T (n.486-29083G>T) c.457C>A (p.Arg153=) c.772C>A (p.Arg258=) c.727C>A (p.Arg243=) c.634C>A (p.Arg212=) | |
| 9 | g.36234116A>C | CA464496088 | CLTA,GNE | c.879T>G (p.Val293=) c.609T>G (p.Val203=) c.786T>G (p.Val262=) c.486-29082A>C (n.486-29082A>C) c.456T>G (p.Val152=) c.771T>G (p.Val257=) c.726T>G (p.Val242=) c.633T>G (p.Val211=) | |
| 9 | g.36234116A>G | CA464496089 | CLTA,GNE | c.879T>C (p.Val293=) c.609T>C (p.Val203=) c.786T>C (p.Val262=) c.486-29082A>G (n.486-29082A>G) c.456T>C (p.Val152=) c.771T>C (p.Val257=) c.726T>C (p.Val242=) c.633T>C (p.Val211=) | |
| 9 | g.36234116A>T | CA464496090 | CLTA,GNE | c.879T>A (p.Val293=) c.609T>A (p.Val203=) c.786T>A (p.Val262=) c.486-29082A>T (n.486-29082A>T) c.456T>A (p.Val152=) c.771T>A (p.Val257=) c.726T>A (p.Val242=) c.633T>A (p.Val211=) | |
| 9 | g.36234117A>C | CA373430879 | CLTA,GNE | c.878T>G (p.Val293Gly) c.608T>G (p.Val203Gly) c.785T>G (p.Val262Gly) c.486-29081A>C (n.486-29081A>C) c.455T>G (p.Val152Gly) c.770T>G (p.Val257Gly) c.725T>G (p.Val242Gly) c.632T>G (p.Val211Gly) | |
| 9 | g.36234117A>G | CA373430877 | CLTA,GNE | c.878T>C (p.Val293Ala) c.608T>C (p.Val203Ala) c.785T>C (p.Val262Ala) c.486-29081A>G (n.486-29081A>G) c.455T>C (p.Val152Ala) c.770T>C (p.Val257Ala) c.725T>C (p.Val242Ala) c.632T>C (p.Val211Ala) | |
| 9 | g.36234117A>T | CA373430878 | CLTA,GNE | c.878T>A (p.Val293Asp) c.608T>A (p.Val203Asp) c.785T>A (p.Val262Asp) c.486-29081A>T (n.486-29081A>T) c.455T>A (p.Val152Asp) c.770T>A (p.Val257Asp) c.725T>A (p.Val242Asp) c.632T>A (p.Val211Asp) | |
| 9 | g.36234118C>A | CA373430880 | CLTA,GNE | c.877G>T (p.Val293Phe) c.607G>T (p.Val203Phe) c.784G>T (p.Val262Phe) c.486-29080C>A (n.486-29080C>A) c.454G>T (p.Val152Phe) c.769G>T (p.Val257Phe) c.724G>T (p.Val242Phe) c.631G>T (p.Val211Phe) | |
| 9 | g.36234118C>G | CA373430881 | CLTA,GNE | c.877G>C (p.Val293Leu) c.607G>C (p.Val203Leu) c.784G>C (p.Val262Leu) c.486-29080C>G (n.486-29080C>G) c.454G>C (p.Val152Leu) c.769G>C (p.Val257Leu) c.724G>C (p.Val242Leu) c.631G>C (p.Val211Leu) | |
| 9 | g.36234118C>T | CA373430882 | CLTA,GNE | c.877G>A (p.Val293Ile) c.607G>A (p.Val203Ile) c.784G>A (p.Val262Ile) c.486-29080C>T (n.486-29080C>T) c.454G>A (p.Val152Ile) c.769G>A (p.Val257Ile) c.724G>A (p.Val242Ile) c.631G>A (p.Val211Ile) | |
| 9 | g.36234119C>A | CA373430883 | CLTA,GNE | c.876G>T (p.Met292Ile) c.606G>T (p.Met202Ile) c.783G>T (p.Met261Ile) c.486-29079C>A (n.486-29079C>A) c.453G>T (p.Met151Ile) c.768G>T (p.Met256Ile) c.723G>T (p.Met241Ile) c.630G>T (p.Met210Ile) | ClinVar dbSNP |
| 9 | g.36234119C= | CA1846355764 | CLTA,GNE | c.876G= (p.Met292=) c.606G= (p.Met202=) c.783G= (p.Met261=) c.486-29079C= (n.486-29079C=) c.453G= (p.Met151=) c.768G= (p.Met256=) c.723G= (p.Met241=) c.630G= (p.Met210=) | |
| 9 | g.36234119C>G | CA373430884 | CLTA,GNE | c.876G>C (p.Met292Ile) c.606G>C (p.Met202Ile) c.783G>C (p.Met261Ile) c.486-29079C>G (n.486-29079C>G) c.453G>C (p.Met151Ile) c.768G>C (p.Met256Ile) c.723G>C (p.Met241Ile) c.630G>C (p.Met210Ile) | |
| 9 | g.36234119C>T | CA373430885 | CLTA,GNE | c.876G>A (p.Met292Ile) c.606G>A (p.Met202Ile) c.783G>A (p.Met261Ile) c.486-29079C>T (n.486-29079C>T) c.453G>A (p.Met151Ile) c.768G>A (p.Met256Ile) c.723G>A (p.Met241Ile) c.630G>A (p.Met210Ile) | |
| 9 | g.36234120A>C | CA373430887 | CLTA,GNE | c.875T>G (p.Met292Arg) c.605T>G (p.Met202Arg) c.782T>G (p.Met261Arg) c.486-29078A>C (n.486-29078A>C) c.452T>G (p.Met151Arg) c.767T>G (p.Met256Arg) c.722T>G (p.Met241Arg) c.629T>G (p.Met210Arg) | |
| 9 | g.36234120A>G | CA373430888 | CLTA,GNE | c.875T>C (p.Met292Thr) c.605T>C (p.Met202Thr) c.782T>C (p.Met261Thr) c.486-29078A>G (n.486-29078A>G) c.452T>C (p.Met151Thr) c.767T>C (p.Met256Thr) c.722T>C (p.Met241Thr) c.629T>C (p.Met210Thr) |