Transcript #00000109

Transcript name multiple endocrine neoplasia I, transcript variant 1
Gene name MEN1 (menin 1)
Chromosome 11
Transcript - NCBI ID NM_000244.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000235.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

83 entries on 1 page. Showing entries 1 - 83.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-22C>A r.(=) p.(=)
./. - c.-13A>C r.(=) p.(=)
./. - c.-13A>C r.(=) p.(=)
./. - c.-13A>C r.(=) p.(=)
./. - c.-13A>C r.(=) p.(=)
./. - c.-10G>A r.(=) p.(=)
./. - c.-10G>C r.(=) p.(=)
./. - c.-6G>A r.(=) p.(=)
./. - c.30G>T r.(=) p.(=)
./. - c.30G>T r.(=) p.(=)
./. - c.329G>C r.(?) p.(Gly110Ala)
./. - c.541G>T r.(?) p.(Ala181Ser)
./. - c.541G>T r.(?) p.(Ala181Ser)
./. - c.541G>T r.(?) p.(Ala181Ser)
./. - c.541G>T r.(?) p.(Ala181Ser)
./. - c.541G>T r.(?) p.(Ala181Ser)
./. - c.541G>T r.(?) p.(Ala181Ser)
./. - c.541G>T r.(?) p.(Ala181Ser)
./. - c.578C>T r.(?) p.(Pro193Leu)
./. - c.578C>T r.(?) p.(Pro193Leu)
./. - c.578C>T r.(?) p.(Pro193Leu)
./. - c.591G>C r.(?) p.(Gln197His)
./. - c.613G>A r.(?) p.(Gly205Ser)
./. - c.696C>T r.(=) p.(=)
./. - c.700C>T r.(?) p.(Arg234Cys)
./. - c.726G>A r.(=) p.(=)
./. - c.755T>C r.(?) p.(Ile252Thr)
./. - c.777G>A r.(=) p.(=)
./. - c.777G>A r.(=) p.(=)
./. - c.778G>A r.(?) p.(Glu260Lys)
./. - c.798+29G>A r.(=) p.(=)
./. - c.799-36G>A r.(=) p.(=)
./. - c.799-36G>A r.(=) p.(=)
./. - c.799-36G>A r.(=) p.(=)
./. - c.799-15_799-14del r.(=) p.(=)
./. - c.799-15_799-14del r.(=) p.(=)
./. - c.799-10C>T r.(=) p.(=)
./. - c.807C>T r.(=) p.(=)
./. - c.1047G>A r.(=) p.(=)
./. - c.1064+43C>T r.(=) p.(=)
./. - c.1064+43C>T r.(=) p.(=)
./. - c.1095C>T r.(=) p.(=)
./. - c.1145A>G r.(?) p.(Lys382Arg)
./. - c.1192C>G r.(?) p.(Gln398Glu)
./. - c.1221C>A r.(=) p.(=)
./. - c.1245C>T r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1311G>A r.(=) p.(=)
./. - c.1410C>T r.(=) p.(=)
./. - c.1443G>C r.(=) p.(=)
./. - c.1493C>T r.(?) p.(Pro498Leu)
./. - c.1556C>G r.(?) p.(Pro519Arg)
./. - c.1841G>C r.(?) p.(Gly614Ala)
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