Transcript #00025772 (NM_001205293.1, CACNA1E gene)

Transcript name transcript variant 1
Gene name CACNA1E (calcium channel, voltage-dependent, R type, alpha 1E subunit)
Chromosome 1
Transcript - NCBI ID NM_001205293.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001192222.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2022-12-18 12:19:50 +01:00 (CET)
Date last edited N/A


Variants

92 entries on 1 page. Showing entries 1 - 92.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-229C>A r.(?) p.(=)
?/. - c.98C>T r.(?) p.(Ser33Leu)
-?/. - c.124A>C r.(?) p.(Thr42Pro)
-?/. - c.512+24_512+27del r.(=) p.(=)
-?/. - c.952-12397A>G r.(=) p.(=)
-?/. - c.1023T>C r.(?) p.(Phe341=)
-?/. - c.1053C>A r.(?) p.(Ser351=)
-?/. - c.1053C>T r.(?) p.(Ser351=)
+/. - c.1054G>A r.(?) p.(Gly352Arg)
?/. - c.1054G>A r.(?) p.(Gly352Arg)
?/. - c.1145G>T r.(?) p.(Gly382Val)
+?/. - c.1171+1G>T r.spl? p.?
-?/. - c.1215C>A r.(?) p.(Ser405=)
?/. - c.1255C>T r.(?) p.(Arg419Trp)
?/. - c.1274G>C r.(?) p.(Arg425Pro)
-?/. - c.1308C>G r.(?) p.(Ser436=)
+?/. - c.1534G>T r.(?) p.(Glu512*)
-?/. - c.1569G>A r.(?) p.(Met523Ile)
-?/. - c.1935A>G r.(?) p.(Ala645=)
+?/. - c.2069G>T r.(?) p.(Gly690Val)
+?/. - c.2105C>T r.(?) p.(Ala702Val)
-?/. - c.2298-16C>T r.(=) p.(=)
-?/. - c.2477T>G r.(?) p.(Leu826Arg)
?/. - c.2480A>G r.(?) p.(Tyr827Cys)
?/. - c.2483G>A r.(?) p.(Arg828Gln)
?/. - c.2485C>T r.(?) p.(Arg829Ter)
?/. - c.2536G>A r.(?) p.(Glu846Lys)
-?/. - c.2545C>A r.(?) p.(Arg849Ser)
-?/. - c.2555G>A r.(?) p.(Arg852His)
-/. - c.2577T>A r.(?) p.(Asp859Glu)
+?/. - c.2608C>T r.(?) p.(Gln870*)
-?/. - c.2612G>T r.(?) p.(Arg871Met)
-?/. - c.2665C>G r.(?) p.(His889Asp)
-?/. - c.2731C>T r.(?) p.(Arg911Trp)
?/. - c.2731C>T r.(?) p.(Arg911Trp)
-?/. - c.2756G>A r.(?) p.(Arg919Gln)
-?/. - c.2774G>A r.(?) p.(Arg925His)
-?/. - c.2980G>A r.(?) p.(Gly994Arg)
-?/. - c.3055G>A r.(?) p.(Val1019Met)
?/. - c.3184A>G r.(?) p.(Lys1062Glu)
-?/. - c.3207C>T r.(?) p.(Ser1069=)
?/. - c.3320A>T r.(?) p.(Asp1107Val)
?/. - c.3352_3354del r.(?) p.(Lys1118del)
?/. - c.3482T>C r.(?) p.(Leu1161Pro)
?/. - c.3502A>G r.(?) p.(Ile1168Val)
?/. - c.3512C>T r.(?) p.(Ala1171Val)
-?/. - c.3540G>A r.(?) p.(=)
?/. - c.3746G>A r.(?) p.(Arg1249Gln)
?/. - c.3827A>T r.(?) p.(Lys1276Met)
-?/. - c.3837C>T r.(?) p.(Phe1279=)
?/. - c.4030A>G r.(?) p.(Lys1344Glu)
-?/. - c.4089G>T r.(?) p.(Leu1363=)
?/. - c.4191G>A r.(?) p.(Met1397Ile)
+/. - c.4274C>A r.(?) p.(Thr1425Asn)
-?/. - c.4548C>T r.(?) p.(Ala1516=)
-/. - c.4606-7T>C r.(=) p.(=)
-?/. - c.4651A>G r.(?) p.(Ile1551Val)
-?/. - c.4734C>T r.(?) p.(Phe1578=)
?/. - c.4808C>T r.(?) p.(Ser1603Phe)
-?/. - c.4905C>T r.(?) p.(Asp1635=)
+?/. - c.5197T>G r.(?) p.(Ser1733Ala)
-?/. - c.5226C>T r.(?) p.(Asp1742=)
?/. - c.5321C>T r.(?) p.(Pro1774Leu)
?/. - c.5470+1G>T r.spl? p.?
-/. - c.5470+11_5470+15del r.(=) p.(=)
-?/. - c.5711C>T r.(?) p.(Pro1904Leu)
?/. - c.5795G>A r.(?) p.(Arg1932Gln)
-?/. - c.5866G>A r.(?) p.(Asp1956Asn)
-?/. - c.5898+468G>A r.(=) p.(=)
?/. - c.5961G>A r.(?) p.(=)
?/. - c.6056G>A r.(?) p.(Arg2019His)
?/. - c.6095C>T r.(?) p.(Ser2032Leu)
-?/. - c.6115A>G r.(?) p.(Met2039Val)
-?/. - c.6120G>A r.(?) p.(Glu2040=)
?/. - c.6189C>A r.(?) p.(His2063Gln)
?/. - c.6333G>A r.(?) p.(Trp2111*)
?/. - c.6341C>T r.(?) p.(Pro2114Leu)
?/. - c.6347G>A r.(?) p.(Arg2116His)
-/. - c.6347G>A r.(?) p.(Arg2116His)
?/. - c.6359G>A r.(?) p.(Arg2120Lys)
-?/. - c.6359G>A r.(?) p.(Arg2120Lys)
-?/. - c.6400-207A>C r.(=) p.(=)
?/. - c.6440C>G r.(?) p.(Ser2147Cys)
?/. - c.6470G>A r.(?) p.(Arg2157Gln)
?/. - c.6470G>A r.(?) p.(Arg2157Gln)
?/. - c.6496C>A r.(?) p.(Pro2166Thr)
-?/. - c.6535G>A r.(?) p.(Ala2179Thr)
?/. - c.6572_6574del r.(?) p.(Glu2191del)
?/. - c.6734G>T r.(?) p.(Gly2245Val)
?/. - c.6766G>A r.(?) p.(Val2256Met)
?/. - c.6784C>T r.(?) p.(Arg2262Cys)
-?/. - c.6856C>T r.(?) p.(Arg2286Trp)
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