Canonical Allele Identifier: CA395993339
Gene: NUP93 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56836703T>G , CM000678.2:g.56836703T>G GRCh38
NC_000016.9:g.56870615T>G , CM000678.1:g.56870615T>G GRCh37
NC_000016.8:g.55428116T>G NCBI36
NG_052904.1:g.111599T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308159.10:c.1885T>G MANE Select ENSP00000310668.5:p.Tyr629Asp
ENST00000308159.9:c.1885T>G ENSP00000310668.5:p.Tyr629Asp
ENST00000542526.5:c.1516T>G ENSP00000440235.1:p.Tyr506Asp
ENST00000563405.1:c.79T>G ENSP00000458078.1:p.Tyr27Asp
ENST00000564887.5:c.1516T>G ENSP00000458039.1:p.Tyr506Asp
ENST00000569842.5:c.1885T>G ENSP00000458101.1:p.Tyr629Asp
NM_001242795.1:c.1516T>G NP_001229724.1:p.Tyr506Asp
NM_001242796.1:c.1516T>G NP_001229725.1:p.Tyr506Asp
NM_014669.4:c.1885T>G NP_055484.3:p.Tyr629Asp
XM_005256263.2:c.1885T>G XP_005256320.1:p.Tyr629Asp
NM_001242796.2:c.1516T>G NP_001229725.1:p.Tyr506Asp
XM_005256263.3:c.1885T>G XP_005256320.1:p.Tyr629Asp
NM_014669.5:c.1885T>G MANE Select NP_055484.3:p.Tyr629Asp
NM_001242795.2:c.1516T>G NP_001229724.1:p.Tyr506Asp