Transcript #00001372 (NM_000069.2, CACNA1S gene)

Transcript name calcium channel, voltage-dependent, L type, alpha 1S subunit
Gene name CACNA1S (calcium channel, voltage-dependent, L type, alpha 1S subunit)
Chromosome 1
Transcript - NCBI ID NM_000069.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000060.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:29:18 +02:00 (CEST)
Date last edited N/A


Variants

312 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.74C>A r.(?) p.(Pro25Gln)
-/. - c.152+17G>C r.(=) p.(=)
-/. - c.152+32del r.(=) p.(=)
-/. - c.153-61A>T r.(=) p.(=)
?/. - c.153-24G>A r.(=) p.(=)
?/. - c.206C>G r.(?) p.(Ala69Gly)
-/. - c.206C>G r.(?) p.(Ala69Gly)
-?/. - c.206C>G r.(?) p.(Ala69Gly)
-?/. - c.206C>G r.(?) p.(Ala69Gly)
-?/. - c.206C>G r.(?) p.(Ala69Gly)
-/. - c.258+57G>A r.(=) p.(=)
-?/. - c.262A>G r.(?) p.(Lys88Glu)
?/. - c.296T>C r.(?) p.(Ile99Thr)
?/. - c.323A>G r.(?) p.(Tyr108Cys)
-?/. - c.324C>T r.(?) p.(Tyr108=)
?/. - c.329T>A r.(?) p.(Phe110Tyr)
-?/. - c.345C>T r.(?) p.(Asp115=)
-?/. - c.369T>C r.(?) p.(Asn123=)
-?/. - c.398+3G>A r.(?) p.(?)
?/. - c.443A>T r.(?) p.(His148Leu)
+?/. - c.497C>A r.(?) p.(Ala166Asp)
?/. - c.520C>T r.(?) p.(Arg174Trp)
-/. - c.597C>T r.(=) p.(=)
-/. - c.597C>T r.(?) p.(Ile199=)
?/. - c.611del r.(?) p.(Leu204ProfsTer130)
?/. - c.625A>G r.(?) p.(Ile209Val)
?/. - c.625A>G r.(?) p.(Ile209Val)
?/. - c.665T>A r.(?) p.(Met222Lys)
-?/. - c.695-6del r.(=) p.(=)
?/. - c.755G>A r.(?) p.(Arg252His)
-?/. - c.773G>A r.(?) p.(Gly258Asp)
-/. - c.773G>A r.(?) p.(Gly258Asp)
-/. - c.773G>A r.(?) p.(Gly258Asp)
-?/. - c.773G>A r.(?) p.(Gly258Asp)
-?/. - c.773G>A r.(?) p.(Gly258Asp)
-?/. - c.773G>A r.(?) p.(Gly258Asp)
-?/. - c.909T>C r.(?) p.(Asp303=)
+?/. - c.1046C>G r.(?) p.(Thr349Ser)
+?/. - c.1087del r.(?) p.(Leu363PhefsTer5)
-/. - c.1151-38C>A r.(=) p.(=)
-?/. - c.1151-3C>T r.spl? p.?
-?/. - c.1223T>C r.(?) p.(Ile408Thr)
-/. - c.1233-24A>G r.(=) p.(=)
?/. - c.1234C>T r.(?) p.(Arg412Ter)
?/. - c.1234C>T r.(?) p.(Arg412Ter)
?/. - c.1246C>T r.(?) p.(Gln416Ter)
-?/. - c.1246C>T r.(?) p.(Gln416Ter)
?/. - c.1246C>T r.(?) p.(Gln416Ter)
-/. - c.1371T>G r.(=) p.(=)
-/. - c.1371T>G r.(?) p.(Pro457=)
-/. - c.1371T>G r.(?) p.(Pro457=)
-/. - c.1373T>A r.(?) p.(Leu458His)
-/. - c.1373T>A r.(?) p.(Leu458His)
-/. - c.1373T>A r.(?) p.(Leu458His)
?/. - c.1382C>T r.(?) p.(Thr461Ile)
-/. - c.1393+7C>T r.(=) p.(=)
-/. - c.1393+7C>T r.(=) p.(=)
-?/. - c.1393+7C>T r.(=) p.(=)
-?/. - c.1395C>T r.(=) p.(=)
-?/. - c.1452C>T r.(?) p.(Tyr484=)
-/- 11 c.1452C>T r.(?) p.(Tyr484=)
-?/. - c.1458G>A r.(?) p.(Leu486=)
-/. - c.1491C>T r.(=) p.(=)
-/. - c.1491C>T r.(?) p.(Asn497=)
-/- 11 c.1491C>T r.(?) p.(Asn497=)
-/- 11 c.1491C>T r.(?) p.(Asn497=)
+/+ 11 c.1493G>A r.(?) p.(Arg498His)
?/. - c.1493G>T r.(?) p.(Arg498Leu)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/. - c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
+/+ 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
+/+ 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-/. - c.1515T>C r.(=) p.(Cys505=)
-/. - c.1515T>C r.(?) p.(Cys505=)
-/- 11 c.1515T>C r.(?) p.(Cys505=)
-?/. - c.1547C>T r.(?) p.(Ser516Leu)
-/. - c.1548G>A r.(?) p.(=)
+/? 11 c.1551T>C r.(?) p.(Gly571=)
+/+ 11 c.1551T>C r.(?) p.(Gly571=)
-/- 11 c.1551T>C r.(?) p.(Gly571=)
-/- 11 c.1551T>C r.(?) p.(Gly571=)
-/- 11 c.1551T>C r.(?) p.(Gly571=)
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