Transcript #00000192 (NM_020919.3, ALS2 gene)

Transcript name amyotrophic lateral sclerosis 2 (juvenile), transcript variant 1
Gene name ALS2 (amyotrophic lateral sclerosis 2 (juvenile))
Chromosome 2
Transcript - NCBI ID NM_020919.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_065970.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-05-11 13:12:23 +02:00 (CEST)
Date last edited N/A


Variants

188 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-60-56del r.(=) p.(=)
+/. - c.-60-2A>G r.spl? p.?
+?/. - c.-60-2A>G r.spl? p.?
-?/. - c.7T>C r.(?) p.(Ser3Pro)
-/. - c.20+7T>C r.(=) p.(=)
-/. - c.20+7T>C r.(=) p.(=)
-/. - c.20+7T>C r.(=) p.(=)
-/. - c.20+7T>C r.(=) p.(=)
-?/. - c.88A>G r.(?) p.(Ile30Val)
-/. - c.176-18C>T r.(=) p.(=)
?/. - c.217G>A r.(?) p.(Gly73Arg)
-/. - c.280A>G r.(?) p.(Ile94Val)
-?/. - c.280A>G r.(?) p.(Ile94Val)
-?/. - c.280A>G r.(?) p.(Ile94Val)
-/. - c.280A>G r.(?) p.(Ile94Val)
-/. - c.280A>G r.(?) p.(Ile94Val)
-?/. - c.283A>C r.(?) p.(Thr95Pro)
-?/. - c.326A>G r.(?) p.(Asn109Ser)
-?/. - c.326A>G r.(?) p.(Asn109Ser)
?/. - c.331G>A r.(?) p.(Val111Ile)
-?/. - c.339C>T r.(?) p.(Tyr113=)
+/. - c.347G>A r.(?) p.(Gly116Glu)
+/. 4 c.368G>A r.(?) p.(Cys123Tyr)
-?/. - c.384G>C r.(?) p.(Gln128His)
-?/. - c.475G>A r.(?) p.(Glu159Lys)
?/. - c.533G>T r.(?) p.(Cys178Phe)
-?/. - c.812A>G r.(?) p.(His271Arg)
-?/. - c.861A>G r.(?) p.(Glu287=)
+?/. 4 c.880_881del r.(?) p.(Leu294CysfsTer4)
-?/. - c.886G>A r.(?) p.(Ala296Thr)
-?/. - c.886G>A r.(?) p.(Ala296Thr)
-?/. - c.886G>A r.(?) p.(Ala296Thr)
-?/. - c.1037A>G r.(?) p.(Asn346Ser)
-/. - c.1102G>A r.(?) p.(Val368Met)
-/. - c.1102G>A r.(?) p.(Val368Met)
-/. - c.1102G>A r.(?) p.(Val368Met)
-/. - c.1102G>A r.(?) p.(Val368Met)
-/. - c.1102G>A r.(?) p.(Val368Met)
-/. - c.1102G>A r.(?) p.(Val368Met)
-/. - c.1113+202T>G r.(=) p.(=)
-?/. - c.1114-19T>G r.(=) p.(=)
-?/. - c.1115C>G r.(?) p.(Pro372Arg)
?/. - c.1115C>G r.(?) p.(Pro372Arg)
-?/. - c.1115C>G r.(?) p.(Pro372Arg)
?/. - c.1115C>G r.(?) p.(Pro372Arg)
-?/. - c.1472-20del r.(=) p.(=)
-?/. - c.1472-20del r.(=) p.(=)
-?/. - c.1533C>T r.(?) p.(Pro511=)
-?/. - c.1548A>G r.(?) p.(Glu516=)
-?/. - c.1578A>G r.(?) p.(Thr526=)
-?/. - c.1584G>A r.(?) p.(Val528=)
?/. - c.1627G>A r.(?) p.(Asp543Asn)
+/. - c.1640+1G>A r.spl p.?
+/. - c.1640+1G>A r.spl p.?
-?/. - c.1641G>A r.(?) p.(Arg547=)
-?/. - c.1641G>A r.(?) p.(Arg547=)
?/. - c.1649C>T r.(?) p.(Pro550Leu)
-?/. - c.1677A>G r.(?) p.(Lys559=)
-?/. - c.1677A>G r.(?) p.(Lys559=)
-?/. - c.1677A>G r.(?) p.(Lys559=)
+/. - c.1737+1G>A r.spl? p.?
-?/. - c.1737+34T>A r.(=) p.(=)
-?/. - c.1782C>T r.(?) p.(Ser594=)
-?/. - c.1816-8C>T r.(=) p.(=)
-/. - c.1816-8C>T r.(=) p.(=)
-?/. - c.1816-8C>T r.(=) p.(=)
-?/. - c.1887A>G r.(?) p.(Glu629=)
-?/. - c.1919G>A r.(?) p.(Arg640Gln)
?/. - c.2048T>C r.(?) p.(Leu683Ser)
-?/. - c.2088C>T r.(?) p.(His696=)
+/. - c.2143C>T r.(?) p.(Gln715Ter)
?/. - c.2171-3T>G r.(2170_2171insag,=) p.(Asn725GlufsTer16,=)
?/. - c.2171-3T>G r.(2170_2171insag,=) p.(Asn725GlufsTer16,=)
-?/. - c.2241C>T r.(?) p.(Tyr747=)
-?/. - c.2241C>T r.(?) p.(Tyr747=)
-?/. - c.2241C>T r.(?) p.(Tyr747=)
?/. - c.2341A>G r.(?) p.(Ser781Gly)
+?/. - c.2359A>C r.(?) p.(Thr787Pro)
-/. - c.2466G>A r.(?) p.(Val822=)
-/. - c.2466G>A r.(?) p.(Val822=)
-/. - c.2466G>A r.(?) p.(Val822=)
-/. - c.2466G>A r.(?) p.(Val822=)
-/. - c.2466G>A r.(?) p.(Val822=)
-/. - c.2466G>A r.(?) p.(Val822=)
-?/. - c.2479A>T r.(?) p.(Thr827Ser)
-?/. - c.2479A>T r.(?) p.(Thr827Ser)
-?/. - c.2479A>T r.(?) p.(Thr827Ser)
-?/. - c.2528G>A r.(?) p.(Arg843Gln)
-?/. - c.2574T>A r.(?) p.(Phe858Leu)
-/. - c.2581-24del r.(=) p.(=)
-?/. - c.2581-22del r.(=) p.(=)
-?/. - c.2581-20C>T r.(=) p.(=)
-?/. - c.2651G>A r.(?) p.(Arg884Lys)
?/. - c.2681G>A r.(?) p.(Gly894Asp)
?/. - c.2712G>A r.(?) p.(Thr904=)
?/. - c.2712G>A r.(?) p.(Thr904=)
-/. - c.2796C>T r.(?) p.(Ser932=)
-/. - c.2796C>T r.(?) p.(Ser932=)
-/. - c.2796C>T r.(?) p.(Ser932=)
-/. - c.2796C>T r.(?) p.(Ser932=)
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