Transcript #00004241 (NM_000721.3, CACNA1E gene)

Transcript name transcript variant 3
Gene name CACNA1E (calcium channel, voltage-dependent, R type, alpha 1E subunit)
Chromosome 1
Transcript - NCBI ID NM_000721.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000712.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

130 entries on 2 pages. Showing entries 1 - 100.
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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.616+3G>A r.= p.=
+/. 5 c.683T>C r.(?) (p.Leu228Pro)
-?/. - c.952-12397A>G r.(=) p.(=)
-?/. - c.1023T>C r.(?) p.(Phe341=)
+/. 7 c.1042G>C r.(?) (p.Gly348Arg)
-?/. - c.1053C>A r.(?) p.(Ser351=)
-?/. - c.1053C>T r.(?) p.(Ser351=)
+/. 7 c.1054G>A r.(?) (p.Gly352Arg)
+/. 7 c.1054G>A r.(?) (p.Gly352Arg)
+/. 7 c.1054G>A r.(?) (p.Gly352Arg)
+/. 7 c.1054G>A r.(?) (p.Gly352Arg)
+/. 7 c.1054G>A r.(?) (p.Gly352Arg)
+/. 7 c.1054G>A r.(?) (p.Gly352Arg)
+/. 7 c.1054G>A r.(?) (p.Gly352Arg)
+/. 7 c.1054G>A r.(?) (p.Gly352Arg)
+/. 7 c.1054G>A r.(?) (p.Gly352Arg)
+/. - 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)
+/. 14 c.1807A>C r.(?) (p.Ile603Leu)
-?/. - c.1935A>G r.(?) p.(Ala645=)
+/. 16 c.2069G>A r.(?) (p.Gly690Asp)
+?/. - c.2069G>T r.(?) p.(Gly690Val)
+/. 17 c.2093T>C r.(?) (p.Phe698Ser)
+?/. - c.2093T>C r.(?) p.(Phe698Ser)
+/. 17 c.2098G>A r.(?) (p.Ala700Thr)
+/. 17 c.2101A>G r.(?) (p.Ile701Val)
+/. 17 c.2101A>G r.(?) (p.Ile701Val)
+/. 17 c.2101A>G r.(?) (p.Ile701Val)
+/. 17 c.2104G>A r.(?) (p.Ala702Thr)
+/. 17 c.2104G>A r.(?) (p.Ala702Thr)
+/. 17 c.2104G>A r.(?) (p.Ala702Thr)
+/. 17 c.2104G>A r.(?) (p.Ala702Thr)
+/. 17 c.2104G>A r.(?) (p.Ala702Thr)
+/. 17 c.2104G>A r.(?) (p.Ala702Thr)
+/. 17 c.2104G>C r.(?) (p.Ala702Pro)
+?/. - c.2105C>T r.(?) p.(Ala702Val)
-?/. - c.2298-16C>T r.(=) p.(=)
+?/. - c.2311C>T r.(?) p.(Arg771Cys)
-?/. - c.2477T>G r.(?) p.(Leu826Arg)
?/. - c.2480A>G r.(?) p.(Tyr827Cys)
?/. - c.2483G>A r.(?) p.(Arg828Gln)
+/. - c.2485C>T r.(?) p.(Arg829*)
?/. - 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.2635C>T r.(?) p.(Arg879Trp)
-?/. - 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.4165C>T r.(?) p.(Arg1389*)
?/. - c.4191G>A r.(?) p.(Met1397Ile)
+/. - c.4263_4271delinsG r.(?) p.(Ile1422Hisfs*8)
+/. 30 c.4264A>T r.(?) (p.Ile1422Phe)
+/. - c.4274C>A r.(?) p.(Thr1425Asn)
+/. 30 c.4274C>A r.(?) (p.Thr1425Asn)
+/. 30 c.4274C>A r.(?) (p.Thr1425Asn)
+?/. - c.4288G>A r.(?) p.(Gly1430Arg)
+/. 30 c.4288G>A r.(?) (p.Gly1430Arg)
-?/. - c.4548C>T r.(?) p.(Ala1516=)
-/. - c.4606-7T>C r.(=) p.(=)
?/. - c.4608C>T r.4608c>u p.Asn1536=
-?/. - c.4651A>G r.(?) p.(Ile1551Val)
-?/. - c.4734C>T r.(?) p.(Phe1578=)
?/. - c.4808C>T r.(?) p.(Ser1603Phe)
-?/. - c.4905C>T r.(?) p.(Asp1635=)
+/. 38 c.5159C>G r.(?) (p.Ala1720Gly)
-?/. - c.5226C>T r.(?) p.(Asp1742=)
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