Transcript #00010292 (NM_015158.3, KANK1 gene)

Transcript name transcript variant 1
Gene name KANK1 (KN motif and ankyrin repeat domains 1)
Chromosome 9
Transcript - NCBI ID NM_015158.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_055973.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-300734_*7453764del r.0? p.0?
-?/. - c.9C>T r.(?) p.(His3=)
?/. - c.95T>C r.(?) p.(Phe32Ser)
?/. - c.145G>C r.(?) p.(Val49Leu)
-?/. - c.149A>T r.(?) p.(Asp50Val)
?/. - c.185del r.(?) p.(Asn62ThrfsTer47)
-/. - c.200G>A r.(?) p.(Arg67Gln)
?/. - c.205C>T r.(?) p.(Pro69Ser)
-/. - c.206C>T r.(?) p.(Pro69Leu)
-?/. - c.206C>T r.(?) p.(Pro69Leu)
-?/. - c.221C>T r.(?) p.(Pro74Leu)
-?/. - c.346A>G r.(?) p.(Thr116Ala)
?/. - c.383C>T r.(?) p.(Ser128Leu)
-?/. - c.453C>T r.(?) p.(Asn151=)
?/. - c.476T>A r.(?) p.(Met159Lys)
?/. - c.484C>T r.(?) p.(Arg162Trp)
-?/. - c.511A>G r.(?) p.(Thr171Ala)
-?/. - c.528G>A r.(?) p.(Pro176=)
-?/. - c.561T>C r.(?) p.(Phe187=)
-?/. - c.565G>A r.(?) p.(Gly189Ser)
-?/. - c.565G>A r.(?) p.(Gly189Ser)
-?/. - c.565G>A r.(?) p.(Gly189Ser)
-/. - c.624C>G r.(?) p.(Ala208=)
-?/. - c.630C>G r.(?) p.(His210Gln)
?/. - c.631C>T r.(?) p.(Gln211Ter)
-?/. - c.633G>C r.(?) p.(Gln211His)
-?/. - c.633G>C r.(?) p.(Gln211His)
?/. - c.701C>G r.(?) p.(Ser234Cys)
?/. - c.758C>G r.(?) p.(Thr253Ser)
?/. - c.781C>T r.(?) p.(Gln261Ter)
-?/. - c.818G>A r.(?) p.(Arg273His)
-?/. - c.857T>A r.(?) p.(Val286Glu)
?/. - c.972T>A r.(?) p.(Tyr324Ter)
?/. - c.977C>T r.(?) p.(Ala326Val)
-?/. - c.1057G>A r.(?) p.(Glu353Lys)
-?/. - c.1103G>A r.(?) p.(Arg368Gln)
?/. - c.1189G>T r.(?) p.(Glu397*)
-?/. - c.1196G>A r.(?) p.(Arg399Gln)
-?/. - c.1269G>C r.(?) p.(Lys423Asn)
?/. - c.1318G>A r.(?) p.(Val440Met)
-?/. - c.1344G>C r.(?) p.(Met448Ile)
-?/. - c.1344G>C r.(?) p.(Met448Ile)
?/. - c.1364T>G r.(?) p.(Ile455Ser)
-/. - c.1371G>C r.(?) p.(Leu457=)
-/. - c.1390T>G r.(?) p.(Ser464Ala)
-?/. - c.1448G>A r.(?) p.(Arg483Gln)
-?/. - c.1491G>A r.(?) p.(Ser497=)
-?/. - c.1491G>A r.(?) p.(Ser497=)
-?/. - c.1514C>T r.(?) p.(Thr505Met)
?/. - c.1526C>T r.(?) p.(Pro509Leu)
?/. - c.1616G>A r.(?) p.(Gly539Glu)
?/. - c.1707G>C r.(?) p.(Trp569Cys)
?/. - c.1732C>T r.(?) p.(His578Tyr)
-?/. - c.1760A>G r.(?) p.(Glu587Gly)
-?/. - c.1763T>C r.(?) p.(Met588Thr)
-?/. - c.1961C>A r.(?) p.(Ala654Asp)
-?/. - c.1961C>A r.(?) p.(Ala654Asp)
-?/. - c.1971G>A r.(?) p.(Gln657=)
?/. - c.1991C>T r.(?) p.(Ala664Val)
-?/. - c.2038G>T r.(?) p.(Val680Leu)
-?/. - c.2058C>T r.(?) p.(Thr686=)
-?/. - c.2064G>A r.(?) p.(Thr688=)
-/. - c.2090A>G r.(?) p.(Asn697Ser)
-?/. - c.2132C>A r.(?) p.(Thr711Asn)
?/. - c.2167C>T r.(?) p.(Arg723Cys)
?/. - c.2261T>G r.(?) p.(Val754Gly)
?/. - c.2281G>A r.(?) p.(Val761Met)
-?/. - c.2342G>C r.(?) p.(Cys781Ser)
?/. - c.2389G>A r.(?) p.(Val797Met)
?/. - c.2505_2525del r.(?) p.(Gln837_Glu843del)
-?/. - c.2544G>C r.(?) p.(Leu848=)
-?/. - c.2544G>C r.(?) p.(=)
?/. - c.2557G>A r.(?) p.(Gly853Arg)
?/. - c.2582C>T r.(?) p.(Ser861Phe)
?/. - c.2615C>G r.(?) p.(Ser872Cys)
-?/. - c.2686G>C r.(?) p.(Gly896Arg)
-?/. - c.2686G>C r.(?) p.(Gly896Arg)
+?/. - c.2698+1G>A r.spl p.?
?/. - c.2699-2A>G r.spl? p.?
-?/. - c.2846C>T r.(?) p.(Thr949Met)
-?/. - c.2847G>A r.(?) p.(Thr949=)
?/. - c.2903C>T r.(?) p.(Thr968Ile)
-?/. - c.2954A>G r.(?) p.(Lys985Arg)
-?/. - c.2963A>G r.(?) p.(Asn988Ser)
?/. - c.2972A>G r.(?) p.(Lys991Arg)
?/. - c.3061T>C r.(?) p.(Ser1021Pro)
-?/. - c.3103G>A r.(?) p.(Glu1035Lys)
?/. - c.3126C>A r.(?) p.(Asp1042Glu)
-/. - c.3164T>C r.(?) p.(Ile1055Thr)
?/. - c.3205G>A r.(?) p.(Val1069Ile)
+?/. - c.3208C>T r.(?) p.(Gln1070Ter)
-?/. - c.3213A>T r.(?) p.(Glu1071Asp)
+/. - c.3237C>G r.(?) p.(Ile1079Met)
?/. - c.3240A>G r.(?) p.(=)
-?/. - c.3240A>G r.(?) p.(=)
?/. - c.3332T>C r.(?) p.(Met1111Thr)
-/. - c.3333+4A>C r.spl? p.?
-/. - c.3333+19C>G r.(=) p.(=)
?/. - c.3371G>A r.(?) p.(Arg1124His)
?/. - c.3371G>A r.(?) p.(Arg1124His)
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