Transcript #00000229 (NM_020987.3, ANK3 gene)

Transcript name transcript variant 1
Gene name ANK3 (ankyrin 3, node of Ranvier (ankyrin G))
Chromosome 10
Transcript - NCBI ID NM_020987.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_066267.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-06-18 14:33:49 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-343773C>T r.(?) p.(=)
?/. - c.-343727C>T r.(?) p.(=)
?/. - ?::c.2842-1886 r.? p.?
+/. 25i c.2842-1887::? r.? p.?
+?/. - c.22_25del r.(?) p.(Leu8ArgfsTer6)
+?/. - c.114+1G>A r.spl p.?
+?/. - c.114+1G>A r.spl p.?
-?/. - c.284A>G r.(?) p.(Gln95Arg)
-?/. - c.315+10A>G r.(=) p.(=)
-/. - c.402T>C r.(?) p.(=)
-?/. - c.402T>C r.(=) p.(=)
-?/. - c.402T>C r.(=) p.(=)
-/. - c.468C>G r.(?) p.(=)
-/. - c.514-3C>T r.spl? p.?
-/. - c.514-3C>T r.spl? p.?
-/. - c.756G>A r.(?) p.(=)
?/. - c.770G>A r.(?) p.(Arg257Gln)
?/. - c.773C>T r.(?) p.(Ala258Val)
-?/. - c.864C>T r.(?) p.(Leu288=)
-/. - c.909A>C r.(?) p.(=)
-/. - c.1047C>T r.(?) p.(Cys349=)
-/. - c.1047C>T r.(?) p.(Cys349=)
?/. - c.1069A>T r.(?) p.(Asn357Tyr)
?/. - c.1195-1G>A r.spl? p.?
-/. - c.1218T>C r.(?) p.(=)
?/. - c.1429G>A r.(?) p.(Gly477Ser)
-/. - c.1491+6C>T r.(=) p.(=)
?/. - c.1546C>T r.(?) p.(Gln516*)
?/. - c.1661A>G r.(?) p.(His554Arg)
-/. - c.1668G>A r.(?) p.(=)
-/. - c.1690-6_1690-4dup r.spl? p.?
-/. - c.1690-6_1690-4dup r.spl? p.?
-/. - c.1690-5_1690-4dup r.spl? p.?
-/. - c.1690-5_1690-4dup r.spl? p.?
-/. - c.1690-4del r.spl? p.?
-/. - c.1690-4del r.spl? p.?
-/. - c.1690-4del r.spl? p.?
-/. - c.1690-4dup r.spl? p.?
-/. - c.1690-4dup r.spl? p.?
-?/. - c.1690-3C>A r.spl? p.?
?/. - c.1718C>A r.(?) p.(Ala573Glu)
-?/. - c.1745A>G r.(?) p.(Asn582Ser)
?/. - c.1792G>A r.(?) p.(Gly598Arg)
-?/. - c.1825G>A r.(?) p.(Asp609Asn)
?/. - c.1882G>A r.(?) p.(Ala628Thr)
+?/. 17 c.1990G>T r.(?) p.(Gly664*)
?/. - c.2002G>A r.(?) p.(Val668Ile)
?/. - c.2002G>A r.(?) p.(Val668Ile)
?/. - c.2050del r.(?) p.(Leu684SerfsTer7)
-/. - c.2103C>T r.(?) p.(Leu701=)
-?/. - c.2103C>T r.(?) p.(Leu701=)
-/. - c.2124T>C r.(?) p.(=)
-?/. - c.2124T>C r.(=) p.(=)
-?/. - c.2124T>C r.(=) p.(=)
?/. - c.2189G>A r.(?) p.(Gly730Glu)
?/. - c.2293A>G r.(?) p.(Thr765Ala)
-?/. - c.2358C>T r.(?) p.(=)
?/. - c.2375T>C r.(?) p.(Leu792Pro)
-/. - c.2382+6C>A r.(=) p.(=)
?/. - c.2431G>T r.(?) p.(Val811Leu)
-/. - c.2544T>C r.(?) p.(Asp848=)
-/. - c.2544T>C r.(?) p.(Asp848=)
-?/. - c.2551+10T>C r.(=) p.(=)
-/. - c.2565T>C r.(?) p.(=)
-?/. - c.2615-6938A>G r.(=) p.(=)
-/. - c.2615-6882A>G r.(=) p.(=)
-/. - c.2615-6882A>G r.(=) p.(=)
?/. - c.2622T>A r.(?) p.(Asp874Glu)
-?/. - c.2674T>C r.(?) p.(Leu892=)
-/. - c.2727G>A r.(?) p.(=)
?/. - c.2756C>T r.(?) p.(Ser919Leu)
-/. - c.2889C>T r.(?) p.(=)
?/. - c.2911G>A r.(?) p.(Asp971Asn)
-/. - c.3045G>T r.(?) p.(=)
?/. - c.3046G>A r.(?) p.(Ala1016Thr)
-/. - c.3105C>G r.(?) p.(=)
-?/. - c.3126A>G r.(?) p.(=)
-?/. - c.3184G>A r.(?) p.(Val1062Met)
?/. - c.3279T>A r.(?) p.(Phe1093Leu)
?/. - c.3380C>T r.(?) p.(Thr1127Met)
?/. - c.3440T>C r.(?) p.(Ile1147Thr)
?/. - c.3604A>G r.(?) p.(Ile1202Val)
?/. - c.3635T>A r.(?) p.(Phe1212Tyr)
?/. - c.3655A>G r.(?) p.(Thr1219Ala)
?/. - c.3662C>T r.(?) p.(Pro1221Leu)
-?/. - c.3722A>G r.(?) p.(Asn1241Ser)
-/. - c.3822C>G r.(?) p.(=)
?/. - c.3938A>G r.(?) p.(Lys1313Arg)
?/. - c.3999G>A r.(?) p.(Met1333Ile)
-/. - c.4029G>A r.(?) p.(=)
-/. - c.4201-3T>C r.spl? p.?
-/. - c.4351-10dup r.(=) p.(=)
-?/. - c.4400A>G r.(?) p.(Lys1467Arg)
?/. - c.4424C>T r.(?) p.(Pro1475Leu)
-?/. - c.4465C>T r.(?) p.(Pro1489Ser)
+?/. - c.4465C>T r.(?) p.(Pro1489Ser)
?/. - c.4465C>T r.(?) p.(Pro1489Ser)
-?/. - c.4465C>T r.(?) p.(Pro1489Ser)
?/. - c.4465C>T r.(?) p.(Pro1489Ser)
-?/. - c.4698C>T r.(?) p.(=)
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