Paralogue Annotation for CACNA1C residue 1721

Residue details

Gene: CACNA1C
Reference Sequences: LRG: LRG_334, Ensembl variant: ENST00000399655 / ENSP00000382563
Amino Acid Position: 1721
Reference Amino Acid: T - Threonine
Protein Domain: C-terminus


Paralogue Variants mapped to CACNA1C residue 1721

No paralogue variants have been mapped to residue 1721 for CACNA1C.



CACNA1CGGLFGNHV-SYYQSDG--------RSAFPQ>T<FT---T-------QRPLHINKAGSS-QGDT1740
CACNA1AMREMGRDG-YSDSEHYLPMEGQGRAASMPR>L<PA----------------------------2099
CACNA1BVQMQSITRRGPDGEPQPGLESQGRAASMPR>L<AA----------------------------2008
CACNA1DGALLGNHV-NHVNSDR--------RDSLQQ>T<NT---T-------HRPLHVQRPSIPPASDT1744
CACNA1ESVQPSNHG-IYLPSDTQEHAGSGRASSMPR>L<TV----------------------------2006
CACNA1FATMVSQPS-AR---RG--------SGISVS>L<PVGDRL-------PDSLSFG---P------1695
CACNA1GKA--------------Q----SGSVLSVHS>Q<P-----------ADT-----------SYIL2093
CACNA1HT--------------RK----HTFGQRCVS>S<RP---AAP----GGE-----------EAEA2093
CACNA1IHPAVSASQ-KGPEKGTG----TGTLPKIAL>Q<GS---WASLRSPRVN-----------CTLL2007
CACNA1SGGLFGQVD-NFL--ER--------TNSLPP>V<MA---N-------QRPLQFAEIE---MEEM1638
SCN10AKS---------------------------->-<------------------------------1909
SCN11AQT---------------------------->-<------------------------------1772
SCN1AKT---------------------------->-<------------------------------1973
SCN2AKT---------------------------->-<------------------------------1963
SCN3AKT---------------------------->-<------------------------------1958
SCN4APE---------------------------->-<------------------------------1793
SCN5ASS---------------------------->-<------------------------------1965
SCN7A------------------------------>-<------------------------------
SCN8AKK---------------------------->-<------------------------------1935
SCN9AKT---------------------------->-<------------------------------1935
cons                              > <                              

See full Alignment of Paralogues


Known Variants in CACNA1C

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.T1721Sc.5162C>G Putative BenignSIFT: tolerated
Polyphen: benign