Transcript #00024146 (NM_000720.3, CACNA1D gene)

Transcript name transcript variant 1
Gene name CACNA1D (calcium channel, voltage-dependent, L type, alpha 1D subunit)
Chromosome 3
Transcript - NCBI ID NM_000720.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000711.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2016-06-18 11:05:20 +02:00 (CEST)
Date last edited N/A


Variants

281 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-19G>A r.(?) p.(=)
?/. - c.1A>G r.(?) p.(Met1?)
-/. - c.20_22del r.(?) p.(Met7del)
-?/. - c.20_22dup r.(?) p.(Met7dup)
-?/. - c.68-8C>T r.(=) p.(=)
-?/. - c.71C>G r.(?) p.(Ala24Gly)
?/. - c.172G>A r.(?) p.(Asp58Asn)
?/. - c.188C>T r.(?) p.(Ala63Val)
-/. - c.222C>T r.(?) p.(Pro74=)
-/. - c.264C>T r.(?) p.(Tyr88=)
-?/. - c.264C>T r.(?) p.(Tyr88=)
-?/. - c.269_272del r.(?) p.(Lys90ThrfsTer32)
-?/. - c.291G>T r.(?) p.(=)
-/. - c.312C>T r.(?) p.(Arg104=)
?/. - c.320T>G r.(?) p.(Phe107Cys)
-?/. - c.378-7T>A r.(=) p.(=)
-?/. - c.391T>C r.(?) p.(Phe131Leu)
?/. - c.484-1857C>T - -
-?/. - c.484-17T>A r.(=) p.(=)
-?/. - c.484-4A>G r.spl? p.?
-/. - c.546G>A r.(?) p.(Ala182=)
-/. - c.623+8T>A r.(=) p.(=)
-?/. - c.645A>G r.(?) p.(Glu215=)
-/. - c.648A>G r.(?) p.(Gln216=)
-?/. - c.648A>G r.(?) p.(Gln216=)
-?/. - c.648A>G r.(?) p.(Gln216=)
?/. - c.648A>G r.(?) p.(Gln216=)
?/. - c.687C>T r.(?) p.(Gly229=)
-/. - c.723C>T r.(?) p.(Ala241=)
?/. - c.736C>T r.(?) p.(Arg246*)
-/. - c.762G>A r.(?) p.(Val254=)
-?/. - c.766+18_766+20del r.(=) p.(=)
-?/. - c.767-12dup r.(=) p.(=)
-/. - c.767-12dup r.(=) p.(=)
-/. - c.846C>T r.(?) p.(Ile282=)
?/. - c.859A>G r.(?) p.(Ile287Val)
-?/. - c.900A>G r.(?) p.(Thr300=)
-/. - c.920-17G>C r.(=) p.(=)
-/. - c.927A>G r.(?) p.(Val309=)
-?/. - c.954G>A r.(?) p.(Ala318=)
-/. - c.954G>A r.(?) p.(Ala318=)
?/. - c.1003A>C r.(?) p.(Ser335Arg)
?/. - c.1007G>A r.(?) p.(Gly336Asp)
?/. - c.1033A>C r.(?) p.(Thr345Pro)
./. 7 c.1104T>C r.(=) p.(=)
-/. - c.1104T>C r.(?) p.(Asp368=)
-/. - c.1104T>C r.(?) p.(Asp368=)
?/. - c.1112A>C r.(?) p.(Tyr371Ser)
?/. - c.1112A>C r.(?) p.(Tyr371Ser)
?/. - c.1112A>C r.(?) p.(Tyr371Ser)
./. 7i c.1117-600G>C r.(=) p.(=)
./. 7i c.1117-600G>C r.(?) p.(=)
./. 7i c.1117-600G>C r.(=) p.(=)
+?/+? 7i c.1117-600G>C r.(=) p.(=)
-?/. - c.1117-595A>G r.(=) p.(=)
?/. - c.1127C>T r.(?) p.(Ala376Val)
+/. 8 c.1201G>C r.(?) p.(Val401Leu)
+/. 8 c.1207G>C r.1207g>c p.Gly403Arg
+/. 8 c.1208G>A r.(?) p.(Gly403Asp)
+/+ 8 c.1208G>A r.(?) p.(Gly403Asp)
+/. 8 c.1208_1209insGGG r.(?) p.(Gly403dup)
+/. 8 c.1208_1209insGGG r.(?) p.(Gly403dup)
+/. 8 c.1208_1209insGGG r.(?) p.(Gly403dup)
+/. 8 c.1208_1209insGGG r.(?) p.Gly403dup
+/+ 8 c.1208_1209insGGG r.(?) p.(Gly403dup)
+/+ 8 c.1219G>A r.(?) p.(Gly407Arg)
?/. - c.1220+5G>A r.spl? p.?
-/. - c.1220+10C>T r.(=) p.(=)
-?/. - c.1233G>A r.(?) p.(Lys411=)
?/. - c.1291C>A r.(?) p.(Leu431Met)
-?/. - c.1344C>T r.(?) p.(Ile448=)
-/. - c.1344C>T r.(?) p.(Ile448=)
-?/. - c.1344C>T r.(?) p.(Ile448=)
-/. - c.1350G>A r.(?) p.(Pro450=)
-?/. - c.1351G>C r.(?) p.(Glu451Gln)
?/. - c.1385G>A r.(?) p.(Arg462Gln)
?/. - c.1385G>A r.(?) p.(Arg462Gln)
-?/. - c.1407C>T r.(?) p.(Ser469=)
-/. - c.1407C>T r.(?) p.(Ser469=)
?/. - c.1457G>A r.(?) p.(Arg486Gln)
-?/. - c.1469G>A r.(?) p.(Gly490Glu)
?/. - c.1478+4A>C r.spl? p.?
?/. - c.1480T>C r.(?) p.(Cys494Arg)
+?/. 11 c.1493G>T r.(?) p.(Arg498Leu)
-?/. - c.1577G>A r.(?) p.(Arg526His)
-?/. - c.1650C>T r.(?) p.(Ile550=)
-/. - c.1650C>T r.(?) p.(Ile550=)
?/. - c.1697A>G r.(?) p.(Asn566Ser)
?/. - c.1697A>G r.(?) p.(Asn566Ser)
-?/. - c.1764C>T r.(?) p.(Cys588=)
-?/. - c.1771C>T r.(?) p.(Leu591=)
?/. - c.1865C>T r.(?) p.(Thr622Met)
?/. - c.1865C>T r.(?) p.(Thr622Met)
?/. - c.1865C>T r.(?) p.(Thr622Met)
?/. - c.1981G>A r.(?) p.(Ala661Thr)
?/. - c.1999A>T r.(?) p.(Met667Leu)
?/. - c.1999A>T r.(?) p.(Met667Leu)
-?/. - c.2058G>A r.(?) p.(Leu686=)
-/. - c.2058G>A r.(?) p.(Leu686=)
-?/. - c.2058G>A r.(?) p.(Leu686=)
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