No paralogue variants have been mapped to residue 13 for KCNH2.
| KCNH2 | ----------------RR----G-HVAPQN>T<FLDTI---IR----KFEGQSRK-------- | 28 |
| KCNH1 | ----------------RR----G-LVAPQN>T<FLENI---VR----RS--NDTN-------- | 29 |
| KCNH3 | ----------------MR----G-LLAPQN>T<FLDTI---AT----RFDGTHSN-------- | 28 |
| KCNH4 | ----------------MK----G-LLAPQN>T<FLDTI---AT----RFDGTHSN-------- | 28 |
| KCNH5 | ----------------KR----G-LVAPQN>T<FLENI---VR----RS--SESS-------- | 27 |
| KCNH6 | ----------------RR----G-HVAPQN>T<YLDTI---IR----KFEGQSRK-------- | 28 |
| KCNH7 | ----------------RR----G-HVAPQN>T<FLGTI---IR----KFEGQNKK-------- | 28 |
| KCNH8 | ----------------MK----G-LLAPQN>T<FLDTI---AT----RFDGTHSN-------- | 28 |
| CNGA1 | ----------------SMK---NNIINTQQ>S<FVTMPNVIVP----DIEKE----------- | 30 |
| CNGA2 | ----------------K--------TNGVK>-<-------SSP----AN-------------- | 14 |
| CNGA3 | -------------------------INTQY>-<-------SHP----SRTH------------ | 15 |
| CNGA4 | ------------------------------>-<------------------------------ | |
| CNGB1 | ESESMPPEESFKEEEVAV-----ADPSPQE>T<KEAAL---TSTISLRAQGAEISEMNSPSRR | 101 |
| CNGB3 | ------------------------------>-<------------------------------ | |
| HCN1 | ----------------G------------->-<---------------GKPNS---------- | 9 |
| HCN2 | ------------------------------>-<--RG-----G----GGRPGE---------- | 12 |
| HCN3 | ----------------E------------->-<---------------QRPAA---------- | 9 |
| HCN4 | ----------------LPPSMRKRLYSLPQ>Q<VGAK-----A----WIMDEE---------- | 29 |
| cons | > < |
| Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
|---|---|---|---|---|---|
| p.T13N | c.38C>A | Inherited Arrhythmia | LQTS | SIFT: Polyphen: |