Paralogue Annotation for CACNA1C residue 1796

Residue details

Gene: CACNA1C
Reference Sequences: LRG: LRG_334, Ensembl variant: ENST00000399655 / ENSP00000382563
Amino Acid Position: 1796
Reference Amino Acid: P - Proline
Protein Domain: C-terminus


Paralogue Variants mapped to CACNA1C residue 1796

No paralogue variants have been mapped to residue 1796 for CACNA1C.



CACNA1CANNTALGRLPRPAG----YPSTVSTVEGHG>P<PLSPAIR--VQEVAWKLSSNRCHSRESQAA1824
CACNA1A---ENQRRRGRPR----------GNNLSTI>S<DTSPMKRSASVL-------G---PKARRLD2137
CACNA1B---ETQ-----P-----------------V>T<DASPMKRSISTL-------AQ-RPRGTHLC2036
CACNA1DANMSKAAHGKRPSIGNLEHVSENGHHSSHK>H<DREPQRRSSVKRTRYYETYIRSDSGDEQLP1841
CACNA1E---DPQ----------------------VV>T<DPSSMRRSFSTI-------RDKRSN-----2030
CACNA1FAGSNTHRRGSG------------------->-<--------------ALIFTIPEEGNSQPKG1739
CACNA1G--RSPL------------------AQRPLR>R<QAAIRTDSLDVQ-------GL-GSREDLLA2154
CACNA1H------------------------------>-<------------------------------
CACNA1I--SLT------------------------->-<--LSDSP-----------------------2042
CACNA1SAN---------------------------->-<------------------------------1665
SCN10A------------------------------>-<------------------------------
SCN11A------------------------------>-<------------------------------
SCN1A------------------------------>-<------------------------------
SCN2A------------------------------>-<------------------------------
SCN3A------------------------------>-<------------------------------
SCN4A------------------------------>-<------------------------------
SCN5A------------------------------>-<------------------------------
SCN7A------------------------------>-<------------------------------
SCN8A------------------------------>-<------------------------------
SCN9A------------------------------>-<------------------------------
cons                              > <                              

See full Alignment of Paralogues


Known Variants in CACNA1C

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.P1796Lc.5387C>T Putative Benignrs199999203SIFT: tolerated
Polyphen: benign
p.P1796Tc.5386C>A Putative BenignSIFT:
Polyphen: