Transcript #00024572 (NM_153638.2, PANK2 gene)

Transcript name Manually created transcript
Gene name PANK2 (pantothenate kinase 2)
Chromosome 20
Transcript - NCBI ID NM_153638.2
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

55 entries on 1 page. Showing entries 1 - 55.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-11G>A -11 r.(=) p.(=) - utr-5 -
./. - c.332T>A 332 r.(?) p.(Leu111Gln) - missense -
./. - c.332T>A 332 r.(?) p.(Leu111Gln) - missense -
./. - c.332T>A 332 r.(?) p.(Leu111Gln) - missense -
./. - c.332T>A 332 r.(?) p.(Leu111Gln) - missense -
./. - c.332T>A 332 r.(?) p.(Leu111Gln) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.377G>C 377 r.(?) p.(Gly126Ala) - missense -
./. - c.628+30C>G 628 r.(=) p.(=) - intron 30
./. - c.628+30C>G 628 r.(=) p.(=) - intron 30
./. - c.628+30C>G 628 r.(=) p.(=) - intron 30
./. - c.628+35C>T 628 r.(=) p.(=) - intron 35
./. - c.628+35C>T 628 r.(=) p.(=) - intron 35
./. - c.628+35C>T 628 r.(=) p.(=) - intron 35
./. - c.628+35C>T 628 r.(=) p.(=) - intron 35
./. - c.628+35C>T 628 r.(=) p.(=) - intron 35
./. - c.628+42C>A 628 r.(=) p.(=) - intron 42
./. - c.1413-21_1413-20insT 1413 r.(=) p.(=) - intron 20
./. - c.1413-21_1413-20insT 1413 r.(=) p.(=) - intron 20
./. - c.1413-21_1413-20insT 1413 r.(=) p.(=) - intron 20
./. - c.1413-21_1413-20insT 1413 r.(=) p.(=) - intron 20
./. - c.*39G>A 1752 r.(=) p.(=) - utr-3 -
./. - c.*56_*57insT 1769 r.(=) p.(=) - utr-3 -
./. - c.*56_*57insT 1769 r.(=) p.(=) - utr-3 -
./. - c.*56_*57insT 1769 r.(=) p.(=) - utr-3 -
./. - c.*56_*57insT 1769 r.(=) p.(=) - utr-3 -
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