Paralogue Annotation for CACNA1C residue 558

Residue details

Gene: CACNA1C
Reference Sequences: LRG: LRG_334, Ensembl variant: ENST00000399655 / ENSP00000382563
Amino Acid Position: 558
Reference Amino Acid: T - Threonine
Protein Domain: TM domain 2


Paralogue Variants mapped to CACNA1C residue 558

No paralogue variants have been mapped to residue 558 for CACNA1C.



CACNA1CWLVIFLVFLNTLTIASEHYNQPNWLTEVQD>T<ANKALLALFTAEMLLKMYSLGLQAYFVSLF588
CACNA1AWTVLSLVALNTLCVAIVHYNQPEWLSDFLY>Y<AEFIFLGLFMSEMFIKMYGLGTRPYFHSSF551
CACNA1BWVVLCVVALNTLCVAMVHYNQPRRLTTTLY>F<AEFVFLGLFLTEMSLKMYGLGPRSYFRSSF547
CACNA1DWLVIVLVFLNTLTISSEHYNQPDWLTQIQD>I<ANKVLLALFTCEMLVKMYSLGLQAYFVSLF607
CACNA1EWIVLSLVALNTACVAIVHHNQPQWLTHLLY>Y<AEFLFLGLFLLEMSLKMYGMGPRLYFHSSF540
CACNA1FWAVLLLVFLNTLTIASEHHGQPVWLTQIQE>Y<ANKVLLCLFTVEMLLKLYGLGPSAYVSSFF593
CACNA1GRGIMIAILVNTLSMGIEYHEQPEELTNALE>I<SNIVFTSLFALEMLLKLLVYGPFGYIKNPY807
CACNA1HRGIMMAILVNTLSMGVEYHEQPEELTNALE>I<SNIVFTSMFALEMLLKLLACGPLGYIRNPY857
CACNA1IRGIMMAILVNTVSMGIEHHEQPEELTNILE>I<CNVVFTSMFALEMILKLAAFGLFDYLRNPY704
CACNA1SWLVILIVALNTLSIASEHHNQPLWLTRLQD>I<ANRVLLSLFTTEMLMKMYGLGLRQYFMSIF496
SCN10ALTITLCIVVNTIFMAMEHHGMSPTFEAMLQ>I<GNIVFTIFFTAEMVFKIIAFDPYYYFQKKW729
SCN11ALAITICIIINTVFLAMEHHKMEASFEKMLN>I<GNLVFTSIFIAEMCLKIIALDPYHYFRRGW641
SCN1ALAITICIVLNTLFMAMEHYPMTDHFNNVLT>V<GNLVFTGIFTAEMFLKIIAMDPYYYFQEGW832
SCN2ALAITICIVLNTLFMAMEHYPMTEQFSSVLS>V<GNLVFTGIFTAEMFLKIIAMDPYYYFQEGW823
SCN3ALAITICIVLNTLFMAMEHYPMTEQFSSVLT>V<GNLVFTGIFTAEMVLKIIAMDPYYYFQEGW824
SCN4ALGITICIVLNTLFMAMEHYPMTEHFDNVLT>V<GNLVFTGIFTAEMVLKLIAMDPYEYFQQGW642
SCN5ALTITMCIVLNTLFMALEHYNMTSEFEEMLQ>V<GNLVFTGIFTAEMTFKIIALDPYYYFQQGW781
SCN7ALFLIICIILNVCFLTLEHYPMSKQTNTLLN>I<GNLVFIGIFTAEMIFKIIAMHPYGYFQVGW569
SCN8ALAITICIVLNTLFMAMEHHPMTPQFEHVLA>V<GNLVFTGIFTAEMFLKLIAMDPYYYFQEGW817
SCN9ALAITICIVLNTLFMAMEHHPMTEEFKNVLA>I<GNLVFTGIFAAEMVLKLIAMDPYEYFQVGW797
cons                              > <                              

See full Alignment of Paralogues


Known Variants in CACNA1C

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.T558Mc.1673C>T Putative BenignSIFT: tolerated
Polyphen: probably damaging