Transcript #00026036 (NM_001291867.2, NHS gene)

Transcript name transcript variant 3 (removed from reference sequence) (removed from reference sequence) (removed from reference sequence)
Gene name NHS (Nance-Horan syndrome (congenital cataracts and dental anomalies))
Chromosome X
Transcript - NCBI ID NM_001291867.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001278796.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks MANE select
Date created 2025-11-25 18:21:44 +01:00 (CET)
Date last edited N/A


Variants

36 entries on 1 page. Showing entries 1 - 36.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.169C>T r.(?) p.(Pro57Ser)
?/. - c.216_218dup r.(?) p.(Pro73dup)
-?/. - c.348_350dup r.(?) p.(Ala117dup)
?/. - c.457C>T r.(?) p.(Leu153Phe)
-?/. - c.565C>T r.(?) p.(Pro189Ser)
-?/. - c.719-187A>T r.(=) p.(=)
?/. - c.797A>C r.(?) p.(Tyr266Ser)
?/. - c.797A>C r.(?) p.(Tyr266Ser)
-?/. - c.797A>C r.(?) p.(Tyr266Ser)
+/. - c.853-2A>C r.spl p.?
?/. - c.853-1_854dup r.spl? p.?
-?/. - c.961A>C r.(?) p.(Arg321=)
-?/. - c.1041G>A r.(?) p.(Thr347=)
?/. - c.1333A>G r.(?) p.(Arg445Gly)
?/. - c.1434T>A r.(?) p.(His478Gln)
-?/. - c.1438C>T r.(?) p.(Arg480Cys)
?/. - c.1528G>C r.(?) p.(Glu510Gln)
?/. - c.1613A>C r.(?) p.(His538Pro)
-?/. - c.1710C>T r.(?) p.(His570=)
?/. - c.2192_2194del r.(?) p.(Asp731del)
?/. - c.2246G>T r.(?) p.(Gly749Val)
-?/. - c.2820C>T r.(?) p.(Ala940=)
?/. - c.2956T>C r.(?) p.(Ser986Pro)
?/. - c.3253C>A r.(?) p.(Pro1085Thr)
?/. - c.3281T>C r.(?) p.(Leu1094Pro)
?/. - c.3314G>A r.(?) p.(Arg1105His)
-?/. - c.3545C>T r.(?) p.(Pro1182Leu)
-?/. - c.3786G>A r.(?) p.(Thr1262=)
+/. - c.3801_3802del r.(?) p.(Ala1268PhefsTer16)
+/. - c.3801_3802del r.(?) p.(Ala1268PhefsTer16)
+/. - c.3871C>T r.(?) p.(Gln1291*)
-?/. - c.3892G>A r.(?) p.(Glu1298Lys)
?/. - c.4448C>G r.(?) p.(Ser1483Cys)
?/. - c.4529C>A r.(?) p.(Ser1510Tyr)
-?/. - c.4676G>C r.(?) p.(Ser1559Thr)
?/. - c.4711G>A r.(?) p.(Glu1571Lys)
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