No paralogue variants have been mapped to residue 487 for KCNH2.
| KCNH2 | VDIMFIVDI-LINFRTTYVN-ANEEVVSHP>G<RIAVHYFKGW-FLIDMVAAIPFDLLIFGSG | 516 |
| KCNH1 | VDVIFLVDI-VLNFHTTFVG-PAGEVISDP>K<LIRMNYLKTW-FVIDLLSCLPYDVINAFEN | 314 |
| KCNH3 | VEVLFILDI-VLNFRTTFVS-KSGQVVFAP>K<SICLHYVTTW-FLLDVIAALPFDLLHAF-K | 324 |
| KCNH4 | VEMLFILDI-ILNFRTTYVS-QSGQVISAP>R<SIGLHYLATW-FFIDLIAALPFDLLYIF-N | 326 |
| KCNH5 | VDVIFLVDI-VLNFHTTFVG-PGGEVISDP>K<LIRMNYLKTW-FVIDLLSCLPYDIINAFEN | 311 |
| KCNH6 | VDIMFVVDI-VINFRTTYVN-TNDEVVSHP>R<RIAVHYFKGW-FLIDMVAAIPFDLLIFRTG | 364 |
| KCNH7 | VDIMFIIDI-LINFRTTYVN-QNEEVVSDP>A<KIAIHYFKGW-FLIDMVAAIPFDLLIFGSG | 515 |
| KCNH8 | VEILFIIDI-ILNFRTTYVS-KSGQVIFEA>R<SICIHYVTTW-FIIDLIAALPFDLLYAF-N | 320 |
| CNGA1 | SDIVYLIDM-FVRTRTGYLE--QGLLVKEE>L<KLINKYKSNLQFKLDVLSLIPTDLLYFKLG | 264 |
| CNGA2 | SDVVYIADL-FIRLRTGFLE--QGLLVKDT>K<KLRDNYIHTLQFKLDVASIIPTDLIYFAVD | 239 |
| CNGA3 | ADVLYVLDV-LVRARTGFLE--QGLMVSDT>N<RLWQHYKTTTQFKLDVLSLVPTDLAYLKVG | 267 |
| CNGA4 | SDLLYLLDM-VVRFHTGFLE--QGILVVDK>G<RISSRYVRTWSFFLDLASLMPTDVVYVRLG | 133 |
| CNGB1 | CDLIYFLDITVFQTRLQFVR--GGDIITDK>K<DMRNNYLKSRRFKMDLLSLLPLDFLYLKVG | 756 |
| CNGB3 | CDIIYLYDMLFIQPRLQFVR--GGDIIVDS>N<ELRKHYRTSTKFQLDVASIIPFDICYLFFG | 318 |
| HCN1 | SDTVFLLDL-IMNFRTGTVNEDSSEIILDP>K<VIKMNYLKSW-FVVDFISSIPVDYIFLIVE | 240 |
| HCN2 | SDTFFLMDL-VLNFRTGIVIEDNTEIILDP>E<KIKKKYLRTW-FVVDFVSSIPVDYIFLIVE | 309 |
| HCN3 | SDTFFLLDL-VLNFRTGIVVEEGAEILLAP>R<AIRTRYLRTW-FLVDLISSIPVDYIFLVVE | 191 |
| HCN4 | SDTFFLIDL-VLNFRTGIVVEDNTEIILDP>Q<RIKMKYLKSW-FMVDFISSIPVDYIFLIVE | 360 |
| cons | > < |
| Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
|---|---|---|---|---|---|
| p.G487S | c.1459G>A | Putative Benign | SIFT: tolerated Polyphen: benign |