Paralogue Annotation for CACNA1C residue 1689

Residue details

Gene: CACNA1C
Reference Sequences: LRG: LRG_334, Ensembl variant: ENST00000399655 / ENSP00000382563
Amino Acid Position: 1689
Reference Amino Acid: A - Alanine
Protein Domain: C-terminus


Paralogue Variants mapped to CACNA1C residue 1689

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
SCN5AE1954KLong QT syndromeLow1 23631430

To assess whether the paralogue annotation here confidently predicts that variation at this residue is pathogenic, it is important to check the reports in the Pubmed links above to ascertain that the mutations in these paralogues have been proved likely to be disease-causing. It is also important to check that the direction of effect of the variant in the paralogue is compatible with your observed phenotype in CACNA1C.



CACNA1C---ISG----DLTAEEE-LD-K-AMKEAVS>A<------------------------------1689
CACNA1A---QNALPS-TQLDPGGALM---AHESGLK>E<SPSWVTQRAQEMFQKTGTWSPEQGPPTDMP2057
CACNA1BLR-QKS--S-TSLSNGGAIQ---NQESGIK>E<SVSWGTQRTQDAPHEA-RPPLERGHSTEIP1965
CACNA1D---ISC----DLQDDEP-EE-----TKR-->-<------------------------------1692
CACNA1E---AKALPY-LQQDPVSGL-------SGRS>G<YPSMSPLSPQDIFQLACMDPADDGQFQERQ1964
CACNA1F---LTC----DTEEEEE-EG-----QEGVE>E<------------------------------1652
CACNA1G-DDMHTLLLSALESN-MQPH---PTELPGP>D<LLTVRKSGVSRTHSLPNDSYMCRHGSTAEG2062
CACNA1HGTARSPSLSRLLCRQ-EAVH---TDSLEGK>I<DSPRDTLDPAEPGEKTPVRPVTQGGSLQSP2058
CACNA1IPMRVGDLGECFFPLS-STAVSPDPENFLCE>M<EEIPFNPVRSWLKHDSSQAPPSPFSPDASS1955
CACNA1S---VSG----DLAAEEE-LE-----RAMVE>A<------------------------------1591
SCN10A-----------------------------N>E<------------------------------1901
SCN11A-----------------------------N>G<------------------------------1765
SCN1A-----------------------------N>E<------------------------------1966
SCN2A-----------------------------N>E<------------------------------1956
SCN3A-----------------------------N>G<------------------------------1951
SCN4A-----------------GHE---------N>G<------------------------------1785
SCN5A-----------------------------S>E<------------------------------1954
SCN7A-----------------------------K>E<------------------------------1674
SCN8A-----------------------------N>G<------------------------------1928
SCN9A-----------------------------N>E<------------------------------1928
cons                              > <                              

See full Alignment of Paralogues


Known Variants in CACNA1C

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.A1689Tc.5065G>A Putative BenignSIFT: tolerated
Polyphen: benign