Paralogue Annotation for CACNA1C residue 1386

Residue details

Gene: CACNA1C
Reference Sequences: LRG: LRG_334, Ensembl variant: ENST00000399655 / ENSP00000382563
Amino Acid Position: 1386
Reference Amino Acid: A - Alanine
Protein Domain: TM domain 4


Paralogue Variants mapped to CACNA1C residue 1386

No paralogue variants have been mapped to residue 1386 for CACNA1C.



CACNA1CSFQALPYVALLIVMLFFIYAVIGMQVFGKI>A<LND---TTE-----INRNNNFQTFPQAVLL1408
CACNA1ASFKALPYVCLLIAMLFFIYAIIGMQVFGNI>G<IDVEDEDSDEDEFQITEHNNFRTFFQALML1748
CACNA1BSFKALPYVCLLIAMLFFIYAIIGMQVFGNI>A<LDD---DTS-----INRHNNFRTFLQALML1648
CACNA1DSFQALPYVALLIAMLFFIYAVIGMQMFGKV>A<MRD---NNQ-----INRNNNFQTFPQAVLL1418
CACNA1ESFKALPYVCLLIAMLFFIYAIIGMQVFGNI>K<LDE---ESH-----INRHNNFRSFFGSLML1655
CACNA1FSFQALPYVALLIAMIFFIYAVIGMQMFGKV>A<LQD---GTQ-----INRNNNFQTFPQAVLL1375
CACNA1GALPQVGNLGLLFMLLFFIFAALGVELFGDL>E<CDET---HP--CEGLGRHATFRNFGMAFLT1794
CACNA1HALPQVGNLGLLFMLLFFIYAALGVELFGRL>E<CSED---NP--CEGLSRHATFSNFGMAFLT1800
CACNA1IALPQVGNLGLLFMLLFFIYAALGVELFGKL>V<CNDE---NP--CEGMSRHATFENFGMAFLT1670
CACNA1SSFQALPYVALLIVMLFFIYAVIGMQMFGKI>A<LVD---GTQ-----INRNNNFQTFPQAVLL1315
SCN10ASLPALFNIGLLLFLVMFIYSIFGMSSFPHV>R<W-----EAG-----IDDMFNFQTFANSMLC1653
SCN11ASLPSLFNIGLLLFLIMFIYAILGMNWFSKV>N<P-----ESG-----IDDIFNFKTFASSMLC1543
SCN1ASLPALFNIGLLLFLVMFIYAIFGMSNFAYV>K<R-----EVG-----IDDMFNFETFGNSMIC1716
SCN2ASLPALFNIGLLLFLVMFIYAIFGMSNFAYV>K<R-----EVG-----IDDMFNFETFGNSMIC1706
SCN3ASLPALFNIGLLLFLVMFIYAIFGMSNFAYV>K<K-----EAG-----IDDMFNFETFGNSMIC1701
SCN4ASLPALFNIGLLLFLVMFIYSIFGMSNFAYV>K<K-----ESG-----IDDMFNFETFGNSIIC1528
SCN5ASLPALFNIGLLLFLVMFIYSIFGMANFAYV>K<W-----EAG-----IDDMFNFQTFANSMLC1703
SCN7ASLPALLNIILLIFLVMFIYAVFGMYNFAYV>K<K-----EAG-----INDVSNFETFGNSMLC1426
SCN8ASLPALFNIGLLLFLVMFIFSIFGMSNFAYV>K<H-----EAG-----IDDMFNFETFGNSMIC1697
SCN9ASLPALFNIGLLLFLVMFIYAIFGMSNFAYV>K<K-----EDG-----INDMFNFETFGNSMIC1679
cons                              > <                              

See full Alignment of Paralogues


Known Variants in CACNA1C

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.A1386Sc.4156G>T Putative BenignSIFT: tolerated
Polyphen: probably damaging