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.56385013_56385022delinsACGAGTTTAT | CA1168547954 | c.759+93864_759+93873delinsATAAACTCGT (n.759+93864_759+93873delinsATAAACTCGT) c.366+15072_366+15081delinsATAAACTCGT c.192+98241_192+98250delinsATAAACTCGT c.378+98241_378+98250delinsATAAACTCGT c.768+98241_768+98250delinsATAAACTCGT | ||
| 1 | g.56385014C>A | CA23054262 | c.759+93872G>T (n.759+93872G>T) c.366+15080G>T c.192+98249G>T c.378+98249G>T c.768+98249G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
| 1 | g.56385014C= | CA1140246332 | c.759+93872G= (n.759+93872G=) c.366+15080G= c.192+98249G= c.378+98249G= c.768+98249G= | ||
| 1 | g.56385014C>G | CA2581668330 | c.759+93872G>C (n.759+93872G>C) c.366+15080G>C c.192+98249G>C c.378+98249G>C c.768+98249G>C | ||
| 1 | g.56385014C>T | CA737156480 | c.759+93872G>A (n.759+93872G>A) c.366+15080G>A c.192+98249G>A c.378+98249G>A c.768+98249G>A | dbSNP gnomAD v3 gnomAD v4 | |
| 1 | g.56385015_56385023del | CA737156478 | c.759+93864_759+93872del (n.759+93864_759+93872del) c.366+15072_366+15080del c.192+98241_192+98249del c.378+98241_378+98249del c.768+98241_768+98249del | dbSNP gnomAD v3 gnomAD v4 | |
| 1 | g.56385015G>A | CA23054263 | c.759+93871C>T (n.759+93871C>T) c.366+15079C>T c.192+98248C>T c.378+98248C>T c.768+98248C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
| 1 | g.56385015G= | CA1168547955 | c.759+93871C= (n.759+93871C=) c.366+15079C= c.192+98248C= c.378+98248C= c.768+98248C= | ||
| 1 | g.56385019T>A | CA2510353874 | c.759+93867A>T (n.759+93867A>T) c.366+15075A>T c.192+98244A>T c.378+98244A>T c.768+98244A>T | ||
| 1 | g.56385022T>A | CA418075549 | c.759+93864A>T (n.759+93864A>T) c.366+15072A>T c.192+98241A>T c.378+98241A>T c.768+98241A>T | dbSNP gnomAD v3 gnomAD v4 | |
| 1 | g.56385022T= | CA1168547956 | c.759+93864A= (n.759+93864A=) c.366+15072A= c.192+98241A= c.378+98241A= c.768+98241A= | ||
| 1 | g.56385024A= | CA1168547957 | c.759+93862T= (n.759+93862T=) c.366+15070T= c.192+98239T= c.378+98239T= c.768+98239T= | ||
| 1 | g.56385024A>G | CA1002011523 | c.759+93862T>C (n.759+93862T>C) c.366+15070T>C c.192+98239T>C c.378+98239T>C c.768+98239T>C | dbSNP gnomAD v3 gnomAD v4 | |
| 1 | g.56385026A= | CA1168547958 | c.759+93860T= (n.759+93860T=) c.366+15068T= c.192+98237T= c.378+98237T= c.768+98237T= | ||
| 1 | g.56385026A>T | CA737156483 | c.759+93860T>A (n.759+93860T>A) c.366+15068T>A c.192+98237T>A c.378+98237T>A c.768+98237T>A | dbSNP gnomAD v3 gnomAD v4 | |
| 1 | g.56385028_56385030delinsAAT | CA1168547959 | c.759+93856_759+93858delinsATT (n.759+93856_759+93858delinsATT) c.366+15064_366+15066delinsATT c.192+98233_192+98235delinsATT c.378+98233_378+98235delinsATT c.768+98233_768+98235delinsATT | ||
| 1 | g.56385030_56385031del | CA23054264 | c.759+93856_759+93857del (n.759+93856_759+93857del) c.366+15064_366+15065del c.192+98233_192+98234del c.378+98233_378+98234del c.768+98233_768+98234del | dbSNP | |
| 1 | g.56385033G>A | CA23054265 | c.759+93853C>T (n.759+93853C>T) c.366+15061C>T c.192+98230C>T c.378+98230C>T c.768+98230C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
| 1 | g.56385033G>C | CA1168547960 | c.759+93853C>G (n.759+93853C>G) c.366+15061C>G c.192+98230C>G c.378+98230C>G c.768+98230C>G | dbSNP | |
| 1 | g.56385033G= | CA1145703941 | c.759+93853C= (n.759+93853C=) c.366+15061C= c.192+98230C= c.378+98230C= c.768+98230C= | ||
| 1 | g.56385034C= | CA1168547961 | c.759+93852G= (n.759+93852G=) c.366+15060G= c.192+98229G= c.378+98229G= c.768+98229G= | ||
| 1 | g.56385034C>T | CA737156484 | c.759+93852G>A (n.759+93852G>A) c.366+15060G>A c.192+98229G>A c.378+98229G>A c.768+98229G>A | dbSNP gnomAD v3 gnomAD v4 | |
| 1 | g.56385035A= | CA1168547962 | c.759+93851T= (n.759+93851T=) c.366+15059T= c.192+98228T= c.378+98228T= c.768+98228T= | ||
| 1 | g.56385035A>G | CA1168547963 | c.759+93851T>C (n.759+93851T>C) c.366+15059T>C c.192+98228T>C c.378+98228T>C c.768+98228T>C | dbSNP | |
| 1 | g.56385036_56385037delinsCA | CA1168547964 | c.759+93849_759+93850delinsTG (n.759+93849_759+93850delinsTG) c.366+15057_366+15058delinsTG c.192+98226_192+98227delinsTG c.378+98226_378+98227delinsTG c.768+98226_768+98227delinsTG | ||
| 1 | g.56385037del | CA737156485 | c.759+93849del (n.759+93849del) c.366+15057del c.192+98226del c.378+98226del c.768+98226del | dbSNP | |
| 1 | g.56385037A= | CA1168547965 | c.759+93849T= (n.759+93849T=) c.366+15057T= c.192+98226T= c.378+98226T= c.768+98226T= | ||
| 1 | g.56385037A>G | CA737156486 | c.759+93849T>C (n.759+93849T>C) c.366+15057T>C c.192+98226T>C c.378+98226T>C c.768+98226T>C | dbSNP gnomAD v3 gnomAD v4 | |
| 1 | g.56385038T>G | CA2598416709 | c.759+93848A>C (n.759+93848A>C) c.366+15056A>C c.192+98225A>C c.378+98225A>C c.768+98225A>C | dbSNP gnomAD v3 gnomAD v4 | |
| 1 | g.56385042T>C | CA2516432577 | c.759+93844A>G (n.759+93844A>G) c.366+15052A>G c.192+98221A>G c.378+98221A>G c.768+98221A>G | ||
| 1 | g.56385046C>A | CA23054266 | c.759+93840G>T (n.759+93840G>T) c.366+15048G>T c.192+98217G>T c.378+98217G>T c.768+98217G>T | dbSNP | |
| 1 | g.56385046C= | CA1168547966 | c.759+93840G= (n.759+93840G=) c.366+15048G= c.192+98217G= c.378+98217G= c.768+98217G= | ||
| 1 | g.56385046C>G | CA1168547967 | c.759+93840G>C (n.759+93840G>C) c.366+15048G>C c.192+98217G>C c.378+98217G>C c.768+98217G>C | dbSNP | |
| 1 | g.56385051C>T | CA645821902 | c.759+93835G>A (n.759+93835G>A) c.366+15043G>A c.192+98212G>A c.378+98212G>A c.768+98212G>A | COSMIC | |
| 1 | g.56385052A= | CA1168547968 | c.759+93834T= (n.759+93834T=) c.366+15042T= c.192+98211T= c.378+98211T= c.768+98211T= | ||
| 1 | g.56385052A>G | CA23054267 | c.759+93834T>C (n.759+93834T>C) c.366+15042T>C c.192+98211T>C c.378+98211T>C c.768+98211T>C | dbSNP | |
| 1 | g.56385054A= | CA1168547969 | c.759+93832T= (n.759+93832T=) c.366+15040T= c.192+98209T= c.378+98209T= c.768+98209T= | ||
| 1 | g.56385054A>G | CA1168547970 | c.759+93832T>C (n.759+93832T>C) c.366+15040T>C c.192+98209T>C c.378+98209T>C c.768+98209T>C | dbSNP | |
| 1 | g.56385059T>C | CA1168547972 | c.759+93827A>G (n.759+93827A>G) c.366+15035A>G c.192+98204A>G c.378+98204A>G c.768+98204A>G | dbSNP | |
| 1 | g.56385059T= | CA1168547971 | c.759+93827A= (n.759+93827A=) c.366+15035A= c.192+98204A= c.378+98204A= c.768+98204A= | ||
| 1 | g.56385067A= | CA1168547974 | c.759+93819T= (n.759+93819T=) c.366+15027T= c.192+98196T= c.378+98196T= c.768+98196T= | ||
| 1 | g.56385067A>C | CA1168547973 | c.759+93819T>G (n.759+93819T>G) c.366+15027T>G c.192+98196T>G c.378+98196T>G c.768+98196T>G | dbSNP | |
| 1 | g.56385071G>C | CA1168547976 | c.759+93815C>G (n.759+93815C>G) c.366+15023C>G c.192+98192C>G c.378+98192C>G c.768+98192C>G | dbSNP | |
| 1 | g.56385071G= | CA1168547975 | c.759+93815C= (n.759+93815C=) c.366+15023C= c.192+98192C= c.378+98192C= c.768+98192C= | ||
| 1 | g.56385078A= | CA1168547977 | c.759+93808T= (n.759+93808T=) c.366+15016T= c.192+98185T= c.378+98185T= c.768+98185T= | ||
| 1 | g.56385079_56385083dup | CA1168547978 | c.759+93803_759+93807dup (n.759+93803_759+93807dup) c.366+15011_366+15015dup c.192+98180_192+98184dup c.378+98180_378+98184dup c.768+98180_768+98184dup | dbSNP | |
| 1 | g.56385080G>C | CA1168547980 | c.759+93806C>G (n.759+93806C>G) c.366+15014C>G c.192+98183C>G c.378+98183C>G c.768+98183C>G | dbSNP | |
| 1 | g.56385080G= | CA1168547979 | c.759+93806C= (n.759+93806C=) c.366+15014C= c.192+98183C= c.378+98183C= c.768+98183C= | ||
| 1 | g.56385083C>A | CA737156488 | c.759+93803G>T (n.759+93803G>T) c.366+15011G>T c.192+98180G>T c.378+98180G>T c.768+98180G>T | dbSNP | |
| 1 | g.56385083C= | CA1168547981 | c.759+93803G= (n.759+93803G=) c.366+15011G= c.192+98180G= c.378+98180G= c.768+98180G= |