Transcript #00000057 (NM_000049.2, ASPA gene)

Transcript name aspartoacylase, transcript variant 2
Gene name ASPA (aspartoacylase)
Chromosome 17
Transcript - NCBI ID NM_000049.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001121557.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-05-11 13:11:57 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/+ 2i c.?del r.(?) p.(?)
+/+ 3 c.?del r.(?) p.(?)
-?/. - c.-4479_-4478del r.(?) p.(=)
+/+ _1_6_ c.0 r.0? p.0?
+/+ _1_6_ c.0 r.0? p.0?
+/+ _1_6_ c.0 r.0? p.0?
+/+ _1_6_ c.0 r.0? p.0?
+/+ 1 c.2T>C r.(?) p.0?
+/+ 1 c.10delinsGG r.(?) p.(Cys4Glyfs*5)
-?/. - c.10T>C r.(?) p.(Cys4Arg)
+/+ 1 c.32del r.(?) p.(Ile11Asnfs*15)
+/+ 1 c.34_46del r.(?) p.(Gln12Serfs*10)
+/+ 1 c.41T>G r.(?) p.(Val14Gly)
+/+ 1 c.47T>C r.(?) p.(Ile16Thr)
+/+ 1 c.47T>C r.(?) p.(Ile16Thr)
+/+ 1 c.52G>A r.(?) p.(Gly18Arg)
+/+ 1 c.62A>C r.(?) p.(His21Pro)
+/+ 1 c.71A>G r.(?) p.(Glu24Gly)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/. - c.79G>A r.(?) p.(Gly27Arg)
?/. - c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.79G>A r.(?) p.(Gly27Arg)
+/+ 1 c.169G>A r.(?) p.(Ala57Thr)
+/+ 1 c.170C>T r.(?) p.(Ala57Val)
+/+ 1 c.203A>C r.(?) p.(Asp68Ala)
+/+ 1 c.209A>G r.(?) p.(Asn70Ser)
+/+ 1 c.212G>A r.(?) p.(Arg71His)
+/+ 1i c.237-2A>T r.spl p.?
+/+ 1i_6_ c.(236+1_237-1)_(*1_?)del r.(?) p.(?)
+/+ 2 c.244del r.(?) p.(Met82Cysfs*9)
+/+ 2 c.244dup r.(?) p.(Met82Asnfs*8)
+/+ 2 c.244dup r.(?) p.(Met82Asnfs*8)
+/+ 2 c.244dup r.(?) p.(Met82Asnfs*8)
+/+ 2 c.244dup r.(?) p.(Met82Asnfs*8)
?/. - c.260C>T r.(?) p.(Pro87Leu)
-?/. - c.294T>C r.(?) p.(His98=)
+/+ 2 c.302G>T r.(?) p.(Gly101Val)
+/+ 2 c.302G>T r.(?) p.(Gly101Val)
+/+ 2 c.327T>G r.(?) p.(Tyr109*)
+/+ 2 c.340G>T r.(?) p.(Asp114Tyr)
+/+ 2 c.342C>A r.(?) p.(Asp114Glu)
+/+ 2 c.362A>T r.(?) p.(Asn121Ile)
+/+ 2 c.368G>A r.(?) p.(Gly123Glu)
+/+ 2 c.382del r.(?) p.(Glu129Argfs*8)
+/+ 2 c.427A>T r.(?) p.(Ile143Phe)
+/+ 2 c.428T>C r.(?) p.(Ile143Thr)
+/+ 2i c.432+1G>A r.(?) p.?
+/+ 2i c.433-2A>G r.spl p.?
+/. - c.433-2A>G r.spl? p.?
+/+ 2i c.433-1G>A r.spl p.?
+/+ 2i_5i c.(432+1_433-1)_(744+1_745-1)del r.? p.?
+/+ 3 c.455G>A r.(?) p.(Cys152Tyr)
+/+ 3 c.456C>G r.(?) p.(Cys152Trp)
?/. - c.460G>A r.(?) p.(Val154Ile)
?/. - c.470T>C r.(?) p.(Ile157Thr)
?/. - c.494C>T r.(?) p.(Ala165Val)
+?/. - c.497C>T r.(?) p.(Thr166Ile)
+/+ 3 c.497C>T r.(?) p.(Thr166Ile)
+/+ 3 c.502C>T r.(?) p.(Arg168Cys)
+/+ 3 c.502C>T r.(?) p.(Arg168Cys)
+/+ 3 c.502C>T r.(?) p.(Arg168Cys)
+/+ 3 c.502C>T r.(?) p.(Arg168Cys)
+/+ 3 c.502C>T r.(?) p.(Arg168Cys)
+/+ 3 c.503G>A r.(?) p.(Arg168His)
+/+ 3 c.503G>A r.(?) p.(Arg168His)
+/+ 3 c.503G>A r.(?) p.(Arg168His)
+/+ 3 c.503G>A r.(?) p.(Arg168His)
+/+ 3 c.503G>A r.(?) p.(Arg168His)
+/+ 3 c.503G>A r.(?) p.(Arg168His)
+/+ 3 c.503G>A r.(?) p.(Arg168His)
+/+ 3 c.503G>A r.(?) p.(Arg168His)
+/+ 3 c.503G>A r.(?) p.(Arg168His)
+/+ 3 c.503G>A r.(?) p.(Arg168His)
+/+ 3 c.503G>A r.(?) p.(Arg168His)
?/. - c.509T>C r.(?) p.(Ile170Thr)
?/. - c.509T>C r.(?) p.(Ile170Thr)
?/. - c.509T>C r.(?) p.(Ile170Thr)
?/. - c.509T>C r.(?) p.(Ile170Thr)
+/+ 3i_4i c.(526+1_527-1)_(634+1_635-1)del r.(?) p.?
+/+ 3i_4i c.(526+1_527-1)_(634+1_635-1)del r.(?) p.?
+/+ 4 c.527_532del r.(?) p.(Gly176_Ile177del)
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