Canonical Allele Identifier: CA395992827
Gene: NUP93 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56836602C>A , CM000678.2:g.56836602C>A GRCh38
NC_000016.9:g.56870514C>A , CM000678.1:g.56870514C>A GRCh37
NC_000016.8:g.55428015C>A NCBI36
NG_052904.1:g.111498C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308159.10:c.1784C>A MANE Select ENSP00000310668.5:p.Pro595His
ENST00000308159.9:c.1784C>A ENSP00000310668.5:p.Pro595His
ENST00000542526.5:c.1415C>A ENSP00000440235.1:p.Pro472His
ENST00000564887.5:c.1415C>A ENSP00000458039.1:p.Pro472His
ENST00000569842.5:c.1784C>A ENSP00000458101.1:p.Pro595His
NM_001242795.1:c.1415C>A NP_001229724.1:p.Pro472His
NM_001242796.1:c.1415C>A NP_001229725.1:p.Pro472His
NM_014669.4:c.1784C>A NP_055484.3:p.Pro595His
XM_005256263.2:c.1784C>A XP_005256320.1:p.Pro595His
NM_001242796.2:c.1415C>A NP_001229725.1:p.Pro472His
XM_005256263.3:c.1784C>A XP_005256320.1:p.Pro595His
NM_014669.5:c.1784C>A MANE Select NP_055484.3:p.Pro595His
NM_001242795.2:c.1415C>A NP_001229724.1:p.Pro472His