Transcript #00023854 (NM_021098.2, CACNA1H gene)

Transcript name transcript variant 1
Gene name CACNA1H (calcium channel, voltage-dependent, T type, alpha 1H subunit)
Chromosome 16
Transcript - NCBI ID NM_021098.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_066921.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2013-11-25 14:24:40 +01:00 (CET)
Date last edited N/A


Variants

424 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.180G>C r.(?) p.(Ala60=)
-?/. - c.180G>C r.(?) p.(Ala60=)
-?/. - c.251G>A r.(?) p.(Gly84Asp)
-/. - c.270C>G r.(?) p.(Arg90=)
?/. - c.299+2T>C r.spl? p.?
-?/. - c.299+14C>G r.(=) p.(=)
-?/. - c.299+14_299+20del r.(=) p.(=)
-?/. - c.299+20_299+40del r.(=) p.(=)
-/. - c.299+20_299+40del r.(=) p.(=)
-/. - c.300-95G>A r.(=) p.(=)
-/. - c.300-85T>A r.(=) p.(=)
-?/. - c.314T>G r.(?) p.(Val105Gly)
-?/. - c.314T>G r.(?) p.(Val105Gly)
?/. - c.346A>T r.(?) p.(Thr116Ser)
-?/. - c.362G>A r.(?) p.(Arg121Gln)
-?/. - c.385G>A r.(?) p.(Gly129Ser)
-/. - c.390C>T r.(?) p.(Ser130=)
-?/. - c.411+18_411+40del r.(=) p.(=)
?/. - c.411+42T>C r.(=) p.(=)
-?/. - c.412-71C>T r.(=) p.(=)
-?/. - c.454G>A r.(?) p.(Val152Ile)
?/. - c.454G>C r.(?) p.(Val152Leu)
-?/. - c.489G>C r.(?) p.(Gln163His)
-/. - c.489G>C r.(?) p.(Gln163His)
-?/. - c.489G>C r.(?) p.(Gln163His)
-/. - c.498C>T r.(=) p.(=)
?/. - c.509C>A r.(?) p.(Thr170Lys)
-?/. - c.546-47C>T r.(=) p.(=)
-/. - c.546-10C>T r.(=) p.(=)
?/. 5 c.567C>G r.(?) p.(Asp189Glu)
?/. - c.577G>T r.(?) p.(Val193Leu)
?/. - c.587C>T r.(?) p.(Ser196Leu)
-/. - c.643+11G>A r.(=) p.(=)
-?/. - c.713T>G r.(?) p.(Phe238Cys)
?/. - c.713T>G r.(?) p.(Phe238Cys)
?/. - c.721T>G r.(?) p.(Phe241Val)
?/. - c.775C>T r.(?) p.(Arg259Cys)
-?/. - c.801C>T r.(?) p.(Val267=)
-?/. - c.804-166A>G r.(=) p.(=)
-?/. - c.819C>T r.(?) p.(Thr273=)
-?/. - c.819C>T r.(?) p.(Thr273=)
-?/. - c.827G>A r.(?) p.(Arg276Gln)
-?/. - c.915C>T r.(?) p.(Ile305=)
-?/. - c.918C>T r.(?) p.(Pro306=)
?/. - c.926G>A r.(?) p.(Arg309His)
-/. - c.937A>G r.(?) p.(Met313Val)
-?/. - c.958G>A r.(?) p.(Glu320Lys)
?/. - c.972G>T r.(?) p.(Gln324His)
-?/. - c.988G>A r.(?) p.(Val330Met)
-?/. - c.988G>A r.(?) p.(Val330Met)
-?/. - c.993C>A r.(?) p.(Gly331=)
-/. - c.994G>A r.(?) p.(Ala332Thr)
-/. - c.994G>A r.(?) p.(Ala332Thr)
-?/. - c.994G>A r.(?) p.(Ala332Thr)
-/. - c.994G>A r.(?) p.(Ala332Thr)
-?/. - c.1029C>T r.(?) p.(Tyr343=)
-?/. - c.1068C>T r.(?) p.(Asn356=)
-/. - c.1107T>C r.(=) p.(=)
-?/. - c.1120-10G>T r.(=) p.(=)
-/. - c.1120-8C>T r.(=) p.(=)
-?/. - c.1120-8C>T r.(=) p.(=)
-/. - c.1120-8C>T r.(=) p.(=)
?/. - c.1127C>T r.(?) p.(Thr376Met)
-?/. - c.1182C>T r.(?) p.(Tyr394=)
?/. - c.1210A>G r.(?) p.(Ile404Val)
-?/. - c.1212+18T>C r.(=) p.(=)
-?/. - c.1212+23G>A r.(=) p.(=)
-?/. - c.1236C>T r.(?) p.(Asn412=)
?/. - c.1300C>T r.(?) p.(Arg434Trp)
-?/. - c.1310G>A r.(?) p.(Arg437Gln)
-?/. - c.1338G>A r.(?) p.(Thr446=)
?/. - c.1352C>T r.(?) p.(Ser451Phe)
-/. - c.1353C>T r.(=) p.(=)
-/. - c.1353C>T r.(?) p.(Ser451=)
-/. - c.1353C>T r.(?) p.(Ser451=)
-?/. - c.1359T>C r.(?) p.(Pro453=)
-?/. - c.1381C>T r.(?) p.(=)
?/. - c.1420C>T r.(?) p.(Arg474Cys)
?/. - c.1421G>C r.(?) p.(Arg474Pro)
-?/. - c.1436A>G r.(?) p.(Tyr479Cys)
?/. - c.1495G>A r.(?) p.(Gly499Ser)
-/. - c.1495G>A r.(?) p.(Gly499Ser)
-?/. - c.1513C>T r.(?) p.(Arg505Cys)
-/. - c.1513C>T r.(?) p.(Arg505Cys)
-?/. - c.1513C>T r.(?) p.(Arg505Cys)
?/. 9 c.1528C>A r.(?) p.(His510Asn)
-?/. - c.1548C>G r.(?) p.(His516Gln)
-?/. - c.1617C>T r.(?) p.(Pro539=)
-?/. - c.1618G>A r.(?) p.(Gly540Ser)
?/. - c.1633G>A r.(?) p.(Ala545Thr)
-?/. - c.1662C>T r.(?) p.(Gly554=)
-?/. - c.1664C>T r.(?) p.(Ala555Val)
-?/. - c.1664C>T r.(?) p.(Ala555Val)
-/. - c.1668C>T r.(?) p.(Pro556=)
-/. - c.1668C>T r.(=) p.(=)
-/. - c.1668C>T r.(?) p.(Pro556=)
-?/. - c.1674G>A r.(?) p.(=)
-?/. - c.1702G>A r.(?) p.(Asp568Asn)
-?/. - c.1753C>T r.(?) p.(Pro585Ser)
-?/. - c.1778_1789del r.(?) p.(His593_Thr597delinsPro)
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