Transcript #00005067 (NM_032436.2, CHAMP1 gene)

Transcript name transcript variant 1
Gene name CHAMP1 (chromosome alignment maintaining phosphoprotein 1)
Chromosome 13
Transcript - NCBI ID NM_032436.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_115812.1
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

41 entries on 1 page. Showing entries 1 - 41.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-178-6_-178-5del r.spl? p.?
-?/. - c.-178-5T>C r.spl? p.?
?/. - c.38G>A r.(?) p.(Arg13His)
-?/. - c.520_522del r.(?) p.(Pro174del)
-?/. - c.520_522del r.(?) p.(Pro174del)
+?/. 3 c.635del r.(?) p.(Pro212Leufs*7)
-?/. - c.915C>T r.(?) p.(Pro305=)
-/. - c.916G>C r.(?) p.(Ala306Pro)
+/. 3 c.958_959del r.(?) p.(Pro320*)
+?/. - c.969G>A r.(?) p.(Trp323Ter)
+/. - c.1001G>A r.(?) p.(Trp334Ter)
+/. 3 c.1002G>A r.(?) p.(Trp334*)
+/. 3 c.1002G>A r.(?) p.(Trp334*)
+/. 3 c.1043G>A r.(?) p.(Trp348*)
+/. - c.1077G>A r.(?) p.(Trp359Ter)
+?/. 3 c.1192C>T r.(?) p.(Arg398*)
+?/. 3 c.1192C>T r.(?) p.(Arg398*)
+?/. - c.1192C>T r.(?) p.(Arg398Ter)
-?/. - c.1209G>C r.(?) p.(Thr403=)
-?/. - c.1366C>T r.(?) p.(Arg456Trp)
-?/. - c.1414T>G r.(?) p.(Ser472Ala)
+/. 3 c.1489C>T r.(?) p.(Arg497*)
+/. 3 c.1489C>T r.(?) p.(Arg497*)
+/. - c.1489C>T r.(?) p.(Arg497Ter)
+?/. 3 c.1559_1560del r.(1559_1560del) p.(Ser520Tyrfs*4)
?/. - c.1606A>C r.(?) p.(Lys536Gln)
?/. - c.1661C>T r.(?) p.(Pro554Leu)
+?/. 3 c.1768C>T r.(?) p.(Gln590*)
+/. - c.1865_1866del r.(?) p.(Asp622Glufs*8)
+?/. 3 c.1866_1867del r.(?) p.(Asp622Glufs*8)
+/. 3 c.1876_1877del r.(?) p.(Ser626Leufs*4)
+/. 3 c.1880C>G r.(?) p.(Ser627*)
-?/. - c.1902T>C r.(?) p.(Ser634=)
+?/. - c.1903_1906del r.(?) p.(Glu635ThrfsTer2)
-?/. - c.1910T>C r.(?) p.(Ile637Thr)
?/. - c.1943G>T r.(?) p.(Gly648Val)
+/. - c.1969C>T r.(?) p.(Gln657Ter)
-?/. - c.2007C>G r.(?) p.(Asn669Lys)
-?/. - c.2193G>A r.(?) p.(Lys731=)
-?/. - c.2306G>A r.(?) p.(Arg769His)
?/. - c.2356C>T r.(?) p.(His786Tyr)
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