Transcript #00009421 (NM_000188.2, HK1 gene)

Transcript name transcript variant 1
Gene name HK1 (hexokinase 1)
Chromosome 10
Transcript - NCBI ID NM_000188.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000179.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.-40237G>C r.? p.?
+?/. - c.-40237G>C r.? p.?
-/. - c.-40225dup r.(?) p.(=)
-?/. - c.-38922G>A r.(=) p.(=)
-?/. - c.-30223A>C r.(?) p.(=)
-/. - c.-30208C>A r.(?) p.(=)
?/. - c.-30201G>A r.(?) p.(=)
+/. - c.-30186C>T r.(=) p.(=)
?/. - c.-30185G>A r.(?) p.(=)
-?/. - c.-30149_-30146dup r.(?) p.(=)
-/. - c.-26662T>A r.(?) p.(=)
-?/. - c.-26633del r.(?) p.(=)
?/. - c.-26633del r.(?) p.(=)
-/. - c.-26621C>T r.(?) p.(=)
-?/. - c.-26593G>A r.(?) p.(=)
-/. - c.-23315G>T r.(?) p.(=)
-?/. - c.-23315G>T r.(?) p.(=)
?/. - c.-23263G>A r.(?) p.(=)
-/. - c.-23252T>C r.(?) p.(=)
-?/. - c.-23252T>C r.(?) p.(=)
-?/. - c.-23245del r.(?) p.(=)
-/. - c.-23245del r.(?) p.(=)
-/. - c.-23245dup r.(?) p.(=)
-?/. - c.-23245dup r.(?) p.(=)
-/. - c.-18189C>G r.(?) p.(=)
-/. - c.-18094A>G r.(?) p.(=)
-/. - c.-18094A>G r.(?) p.(=)
-/. - c.-18083C>T r.(?) p.(=)
-/. - c.-18082G>A r.(?) p.(=)
-?/. - c.-18080A>C r.(?) p.(=)
-/. - c.-18070G>A r.(?) p.(=)
-/. - c.-18070G>A r.(?) p.(=)
-?/. - c.-3186A>G r.(?) p.(=)
+/. - c.-2960C>T r.(?) p.(=)
?/. - c.-2960C>T r.(?) p.(=)
-?/. - c.36G>T r.(?) p.(Thr12=)
-/. - c.78C>G r.(?) p.(Leu26=)
-/. - c.198A>T r.(?) p.(Thr66=)
-/. - c.222C>T r.(?) p.(Gly74=)
-?/. - c.227-20C>T r.(=) p.(=)
?/. - c.250G>A r.(?) p.(Asp84Asn)
?/. - c.352A>G r.(?) p.(Ile118Val)
-/. - c.360C>T r.(?) p.(His120=)
?/. - c.409T>A r.(?) p.(Phe137Ile)
-/. - c.480A>G r.(?) p.(Gln160=)
-?/. - c.495G>A r.(?) p.(Glu165=)
?/. - c.514A>T r.(?) p.(Thr172Ser)
-?/. - c.531G>A r.(?) p.(Ala177=)
-?/. - c.531G>A r.(?) p.(Ala177=)
-?/. - c.534C>T r.(?) p.(Ser178=)
-?/. - c.534C>T r.(?) p.(Ser178=)
?/. - c.605A>G r.(?) p.(Asn202Ser)
+?/. - c.626A>G r.(?) p.(Asp209Gly)
?/. - c.631G>C r.(?) p.(Val211Leu)
-/. - c.691+13C>T r.(=) p.(=)
?/. - c.692-3C>T r.spl? p.?
?/. - c.692-3C>T r.spl? p.?
-/. - c.692-3C>T r.spl? p.?
?/. - c.742G>C r.(?) p.(Val248Leu)
-?/. - c.753C>T r.(?) p.(Asp251=)
-?/. - c.804A>T r.(?) p.(Gly268=)
-?/. - c.828G>A r.(?) p.(Glu276=)
-/. - c.828G>A r.(?) p.(Glu276=)
-?/. - c.828G>A r.(?) p.(Glu276=)
?/. - c.854C>T r.(?) p.(Ser285Phe)
?/. - c.854C>T r.(?) p.(Ser285Phe)
?/. - c.863C>T r.(?) p.(Pro288Leu)
?/. - c.875+1G>A r.spl? p.?
-?/. - c.876-16G>T r.(=) p.(=)
-/. - c.968G>A r.(?) p.(Arg323Gln)
?/. - c.976C>G r.(?) p.(Pro326Ala)
?/. - c.1007C>A r.(?) p.(Thr336Asn)
-/. - c.1031+6T>C r.(=) p.(=)
-?/. - c.1031+7A>G r.(=) p.(=)
-?/. - c.1092C>T r.(?) p.(Ser364=)
?/. - c.1120G>A r.(?) p.(Val374Ile)
?/. - c.1193G>A r.(?) p.(Arg398His)
?/. - c.1196A>G r.(?) p.(Asp399Gly)
?/. - c.1226C>T r.(?) p.(Thr409Met)
-?/. - c.1227G>A r.(?) p.(Thr409=)
-?/. - c.1236C>T r.(?) p.(Val412=)
-?/. - c.1236C>T r.(?) p.(Val412=)
+?/. - c.1240G>A r.(?) p.(Gly414Arg)
+?/. - c.1241G>A r.(?) p.(Gly414Glu)
+?/. - c.1252A>G r.(?) p.(Lys418Glu)
-?/. - c.1265+19A>G r.(=) p.(=)
-/. - c.1265+19A>G r.(=) p.(=)
?/. - c.1266G>T r.(?) p.(Gln422His)
?/. - c.1277G>A r.(?) p.(Arg426His)
?/. - c.1327C>T r.(?) p.(Leu443Phe)
+?/. - c.1334C>T r.(?) p.(Ser445Leu)
+?/. - c.1334C>T r.(?) p.(Ser445Leu)
+/. - c.1334C>T r.(?) p.(Ser445Leu)
+/. - c.1334C>T r.(?) p.(Ser445Leu)
+/. - c.1334C>T r.(?) p.(Ser445Leu)
+/. - c.1334C>T r.(?) p.(Ser445Leu)
+?/. - c.1370C>T r.(?) p.(Thr457Met)
+?/. - c.1370C>T r.(?) p.(Thr457Met)
+?/. - c.1370C>T r.(?) p.(Thr457Met)
-?/. - c.1392C>G r.(?) p.(Ala464=)
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