Transcript #00025791 (NM_001173464.1, KIF21A gene)

Transcript name transcript variant 1
Gene name KIF21A (kinesin family member 21A)
Chromosome 12
Transcript - NCBI ID NM_001173464.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001166935.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2022-12-23 14:47:33 +01:00 (CET)
Date last edited N/A


Variants

68 entries on 1 page. Showing entries 1 - 68.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-4022C>T r.(?) p.(=)
?/. - c.318T>G r.(?) p.(Ile106Met)
-?/. - c.451-6del r.(=) p.(=)
?/. - c.455A>G r.(?) p.(Tyr152Cys)
-?/. - c.600+314T>G r.(=) p.(=)
-?/. - c.1008C>T r.(?) p.(Leu336=)
-?/. - c.1038A>G r.(?) p.(Ala346=)
?/. - c.1054G>C r.(?) p.(Asp352His)
+?/. - c.1067T>C r.(?) p.(Met356Thr)
?/. - c.1072A>T r.(?) p.(Thr358Ser)
-?/. - c.1240G>C r.(?) p.(Gly414Arg)
-?/. - c.1240G>C r.(?) p.(Gly414Arg)
?/. - c.1264T>C r.(?) p.(Phe422Leu)
?/. - c.1270G>C r.(?) p.(Glu424Gln)
+?/. - c.1346T>A r.(?) p.(Leu449Ter)
+?/. - c.1346T>A r.(?) p.(Leu449Ter)
+?/. - c.1346T>A r.(?) p.(Leu449Ter)
-?/. - c.1542G>A r.(?) p.(Ala514=)
-?/. - c.1628A>G r.(?) p.(Lys543Arg)
-?/. - c.1713-11C>G r.(=) p.(=)
-?/. - c.1834G>A r.(?) p.(Asp612Asn)
-?/. - c.1851G>A r.(?) p.(Glu617=)
+?/. - c.1854_1862del r.(?) p.(Glu619_Glu621del)
?/. - c.1860_1862del r.(?) p.(Glu621del)
-/. - c.1880G>T r.(?) p.(Gly627Val)
-?/. - c.1880G>T r.(?) p.(Gly627Val)
-/. - c.1880G>T r.(?) p.(Gly627Val)
-?/. - c.1880G>T r.(?) p.(Gly627Val)
+/. - c.1886G>T r.(?) p.(Ser629Ile)
-?/. - c.2211A>C r.(?) p.(Ala737=)
-?/. - c.2346G>A r.(?) p.(Glu782=)
+?/. - c.2371del r.(?) p.(Arg791GlufsTer8)
+?/. - c.2371del r.(?) p.(Arg791GlufsTer8)
?/. - c.2381A>G r.(?) p.(Glu794Gly)
?/. - c.2407C>T r.(?) p.(Arg803Cys)
?/. - c.2416G>C r.(?) p.(Asp806His)
-?/. - c.2568T>C r.(?) p.(Asp856=)
?/. - c.2663G>C r.(?) p.(Arg888Thr)
-?/. - c.2681C>T r.(?) p.(Thr894Met)
?/. - c.2735G>A r.(?) p.(Arg912Gln)
?/. - c.2759G>A r.(?) p.(Arg920His)
+/. - c.2840T>A r.(?) p.(Met947Lys)
+/. - c.2840T>A r.(?) p.(Met947Lys)
+/. - c.2860C>T r.(?) p.(Arg954Trp)
+/. - c.2860C>T r.(?) p.(Arg954Trp)
+/. - c.2860C>T r.(?) p.(Arg954Trp)
+?/. - c.2899A>G r.(?) p.(Arg967Gly)
+?/. - c.2899A>G r.(?) p.(Arg967Gly)
+?/. - c.2899A>G r.(?) p.(Arg967Gly)
+?/. - c.2899A>G r.(?) p.(Arg967Gly)
+?/. - c.2998_3000del r.(?) p.(Asn1000del)
-?/. - c.3149A>G r.(?) p.(Asn1050Ser)
-?/. - c.3149A>G r.(?) p.(Asn1050Ser)
?/. - c.3218A>G r.(?) p.(Glu1073Gly)
-?/. - c.3306_3319+1dup r.spl? p.?
-?/. - c.3332T>C r.(?) p.(Val1111Ala)
-?/. - c.3492G>A r.(?) p.(Leu1164=)
?/. - c.3538G>A r.(?) p.(Ala1180Thr)
?/. - c.3641C>G r.(?) p.(Pro1214Arg)
-?/. - c.3641C>G r.(?) p.(Pro1214Arg)
?/. - c.3758C>T r.(?) p.(Ser1253Leu)
?/. - c.3926C>A r.(?) p.(Ser1309Tyr)
-?/. - c.3959G>A r.(?) p.(Arg1320Lys)
-?/. - c.4044A>G r.(?) p.(Lys1348=)
?/. - c.4435C>G r.(?) p.(Leu1479Val)
-/. - c.4536T>C r.(?) p.(Thr1512=)
-/. - c.4542C>G r.(?) p.(Ser1514=)
-?/. - c.4562T>G r.(?) p.(Met1521Arg)
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