Transcript #00011983 (NM_152419.2, HGSNAT gene)

Transcript name heparan-alpha-glucosaminide N-acetyltransferase
Gene name HGSNAT (heparan-alpha-glucosaminide N-acetyltransferase)
Chromosome 8
Transcript - NCBI ID NM_152419.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_689632.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

52 entries on 1 page. Showing entries 1 - 52.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.118+32G>C 118 r.(=) p.(=) - intron 32
./. - c.118+32G>C 118 r.(=) p.(=) - intron 32
./. - c.118+32G>C 118 r.(=) p.(=) - intron 32
./. - c.493+46G>T 493 r.(=) p.(=) - intron 46
./. - c.563+50C>T 563 r.(=) p.(=) - intron 50
./. - c.563+50C>T 563 r.(=) p.(=) - intron 50
./. - c.1251-47C>T 1251 r.(=) p.(=) - intron 47
./. - c.1377+20G>A 1377 r.(=) p.(=) - intron 20
./. - c.1377+20G>A 1377 r.(=) p.(=) - intron 20
./. - c.1377+20G>A 1377 r.(=) p.(=) - intron 20
./. - c.1377+20G>A 1377 r.(=) p.(=) - intron 20
./. - c.1377+20G>A 1377 r.(=) p.(=) - intron 20
./. - c.1377+20G>A 1377 r.(=) p.(=) - intron 20
./. - c.1377+20G>A 1377 r.(=) p.(=) - intron 20
./. - c.1377+20G>A 1377 r.(=) p.(=) - intron 20
./. - c.1377+20G>A 1377 r.(=) p.(=) - intron 20
./. - c.1377+20G>A 1377 r.(=) p.(=) - intron 20
./. - c.1567A>C 1567 r.(?) p.(Lys523Gln) - missense -
./. - c.1567A>C 1567 r.(?) p.(Lys523Gln) - missense -
./. - c.1693G>C 1693 r.(?) p.(Gly565Arg) - missense -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1749T>C 1749 r.(?) p.(=) - coding-synonymous -
./. - c.1840G>A 1840 r.(?) p.(Val614Ile) - missense -
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