Paralogue Annotation for CACNA1C residue 1929

Residue details

Gene: CACNA1C
Reference Sequences: LRG: LRG_334, Ensembl variant: ENST00000399655 / ENSP00000382563
Amino Acid Position: 1929
Reference Amino Acid: A - Alanine
Protein Domain: C-terminus


Paralogue Variants mapped to CACNA1C residue 1929

No paralogue variants have been mapped to residue 1929 for CACNA1C.



CACNA1C-Q----------------KTVLPLHLVHHQ>A<LAVAGLSP--LL------------QRSHSP1945
CACNA1A------------------K----------->H<RQHH--------------HHHHHHHHPPPP2224
CACNA1B-EKQRFYSCDRFGGREPPKPK--PSLSSHP>T<SPTAGQEPGPHPQGSGSVNGSPLLSTSGAS2181
CACNA1DPH----------------RTALPLHLMQQQ>I<MAVAGLDS--SK------------AQKYSP1994
CACNA1E-SRCN--SEER-GTQADW-ES--PE-RRQS>R<SPSEGRSQTPNRQGTGSLSESSIPSVSDTS2150
CACNA1F------------------------------>-<----------HR------------GRNSGP1831
CACNA1G------------------------------>-<-L----------------------------2221
CACNA1H------------------------------>-<------------------------------
CACNA1I------------------------------>-<------------------------------
CACNA1S------------------------------>-<LLTQRAMP--RG------------QAPPAP1740
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.A1929Tc.5785G>A Putative Benignrs367594886SIFT: tolerated
Polyphen: benign
p.A1929Sc.5785G>T Putative BenignSIFT:
Polyphen:
p.A1929Vc.5786C>T Putative BenignSIFT:
Polyphen: