Transcript #00026047 (NM_001367721.1, CASK gene)

Transcript name transcript variant 4 (removed from reference sequence) (removed from reference sequence)
Gene name CASK (calcium/calmodulin-dependent serine protein kinase (MAGUK family))
Chromosome X
Transcript - NCBI ID NM_001367721.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001354650.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks MANE select
Date created 2026-02-04 19:30:01 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_3i c.-1959630_278+109del r.0? p.0?
+?/. _1_1i c.(?_-46)_(59+1_60-1)del r.0? p.0?
+?/. _1_1i c.(?_-46)_(59+1_60-1)del r.0? p.0?
+?/. _1_1i c.(?_-46)_(59+1_60-1)del r.0? p.0?
+/. - c.1A>G r.(?) p.(Met1?)
+/. - c.20_27del r.(?) p.(Leu7ArgfsTer35)
+/. - c.37G>T r.(?) p.(Glu13Ter)
+/. - c.45C>A r.(?) p.(Cys15Ter)
+?/. 1i_2i c.(59+1_60-1)_(172+1_173-1)dup r.? p.?
+/. - c.62G>A r.(?) p.(Gly21Asp)
+/. - c.68del r.(?) p.(Phe23SerfsTer18)
+?/. 2 c.77T>A r.(?) p.(Val26Glu)
+/. - c.79C>T r.(?) p.(Arg27Ter)
+/. - c.79C>T r.(?) p.(Arg27Ter)
+/. 2 c.79C>T r.(?) p.(Arg27Ter)
+/. - c.82C>T r.(?) p.(Arg28Ter)
+/. - c.109C>T r.(?) p.(Gln37Ter)
?/. - c.172+1G>A r.spl p.?
+/. - c.184G>A r.(?) p.(Glu62Lys)
-?/. - c.195C>T r.(?) p.(Ile65=)
-?/. - c.195C>T r.(?) p.(Ile65=)
+/. - c.265A>G r.(?) p.(Met89Val)
-/. 3i c.279-6T>A r.spl? p.(?)
+?/. 3i_5i c.(278+1_279-1)_(429+1_430-1)del r.? p.?
?/. - c.294T>G r.(?) p.(Asp98Glu)
+/. - c.316C>T r.(?) p.(Arg106Ter)
+?/. - c.316C>T r.(?) p.(Arg106Ter)
+?/. - c.356+1G>A r.spl p.?
-?/. - c.363T>C r.(?) p.(Tyr121=)
+?/. - c.372_373del r.(?) p.(Gln124HisfsTer10)
+?/. - c.429+1G>A r.spl p.?
?/. - c.429+11419A>G r.spl? p.(?)
?/. - c.429+11487_429+11488del r.(=) p.(?)
-?/. - c.429+11528T>C r.(=) p.(?)
?/. - c.429+11915T>A r.(=) p.(?)
-?/. - c.429+12291T>G r.(=) p.(?)
?/. - c.429+12333G>T r.(=) p.(?)
?/. - c.429+12333G>T r.(=) p.(?)
?/. - c.430-25053G>A r.(=) p.(?)
?/. - c.430-24702T>C r.(=) p.(?)
-?/. - c.430-24576C>G r.(=) p.(?)
?/. - c.430-18160A>G r.(=) p.(?)
?/. - c.430-18160A>G r.(=) p.(?)
-/. - c.430-257T>A r.(=) p.(?)
+?/. 5i_6i c.(429+1_430-1)_(532+1_533-1)del r.? p.?
-?/. - c.444C>T r.(?) p.(Leu148=)
+?/. - c.481G>A r.(?) p.(Gly161Arg)
?/. - c.490G>A r.(?) p.(Gly164Arg)
-?/. - c.532+14A>T r.spl? p.(?)
-?/. - c.532+15A>T r.spl? p.(?)
?/. - c.532+24_532+25dup r.spl? p.(?)
-/. - c.532+25del r.spl? p.(?)
?/. - c.532+25dup r.spl? p.(?)
?/. - c.532+25dup r.spl? p.(?)
?/. - c.532+25dup r.spl? p.(?)
-?/. - c.532+25dup r.spl? p.(?)
?/. - c.532+25dup r.spl? p.(?)
-/. - c.532+114C>A r.spl? p.(?)
+/. - c.532+2768_831+9967dup r.? p.?
+?/. - c.626T>C r.(?) p.(Leu209Pro)
?/. - c.638T>G r.(?) p.(Leu213Arg)
+/. - c.708+1G>A r.spl p.?
+/. - c.708+2T>G r.spl p.?
+/. - c.732del r.(?) p.(His244GlnfsTer9)
+/. - c.763C>T r.(?) p.(Arg255Cys)
?/. - c.802T>C r.(?) p.(Tyr268His)
?/. - c.817C>T r.(?) p.(His273Tyr)
+/. - c.831+1G>A r.spl p.?
+?/. 8i_10i c.(831+1_832-1)_(1015+1_1016-1)del r.? p.?
+/. - c.846C>G r.(?) p.(Tyr282Ter)
+/. - c.858T>G r.(?) p.(Ile286Met)
+/. - c.915+1G>A r.spl p.?
?/. - c.992T>C r.(?) p.(Phe331Ser)
+?/. - c.996_997insT r.(?) p.(Glu333Ter)
+/. - c.1015+1G>A r.spl p.(=)
?/. - c.1016-247dup r.(?) p.(=)
?/. - c.1016-246del r.(?) p.(=)
?/. - c.1016-7C>G r.(?) p.(=)
-?/. - c.1034-3079del r.(?) p.(=)
-?/. - c.1034-1722C>G r.(?) p.(=)
-?/. - c.1034-1688A>T r.(?) p.(=)
-/. - c.1034-6C>T r.(?) p.(=)
-/. - c.1034-6C>T r.(?) p.(=)
-?/. - c.1034-6C>T r.(?) p.(=)
?/. - c.1076C>T r.(?) p.(Ala359Val)
-?/. - c.1077G>A r.(?) p.(Ala359=)
-?/. - c.1104A>G r.(?) p.(Leu368=)
+?/. - c.1105G>C r.(?) p.(Asp369His)
+/. - c.1106_1107insCTCT r.(?) p.(Phe370SerfsTer20)
?/. - c.1116C>G r.(?) p.(His372Gln)
-?/. - c.1156-15T>G r.(?) p.?
+?/. - c.1177_1178del r.(?) p.(Lys393ValfsTer28)
-?/. - c.1186C>T r.(?) p.(Pro396Ser)
?/. - c.1233+2T>C r.spl? p.?
-/. - c.1233+18T>C r.(?) p.(=)
-/. - c.1233+18T>C r.(?) p.(=)
?/. - c.1270G>A r.(?) p.(Asp424Asn)
-?/. - c.1314+18T>C r.(?) p.(=)
+/. 14i c.1315-7A>G r.(1314_1315ins1315-6_1315-1) p.(Als439Hisfs2*)
+/. - c.1315-4_1315-1dup r.spl? p.?
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