Canonical Allele Identifier: CA16603108
Gene: XPO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61492336T>A , CM000664.2:g.61492336T>A GRCh38
NC_000002.11:g.61719471T>A , CM000664.1:g.61719471T>A GRCh37
NC_000002.10:g.61572975T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000401558.7:c.1712A>T MANE Select ENSP00000384863.2:p.Glu571Val
ENST00000451765.6:c.1245+1558A>T ENSP00000413853.2:n.1245+1558A>T
ENST00000469337.2:n.967A>T
ENST00000481073.6:n.1709A>T
ENST00000676553.1:c.1712A>T ENSP00000504247.1:p.Glu571Val
ENST00000676667.1:c.1712A>T ENSP00000503809.1:p.Glu571Val
ENST00000676771.1:c.1667A>T ENSP00000503808.1:p.Glu556Val
ENST00000676778.1:n.1884A>T
ENST00000676783.1:c.*1638A>T ENSP00000503342.1:n.*1638A>T
ENST00000676789.1:c.1712A>T ENSP00000504617.1:p.Glu571Val
ENST00000676889.1:c.1355A>T ENSP00000503075.1:p.Glu452Val
ENST00000676999.1:c.1712A>T ENSP00000502940.1:p.Glu571Val
ENST00000677110.1:n.2279A>T
ENST00000677150.1:c.1712A>T ENSP00000503167.1:p.Glu571Val
ENST00000677157.1:n.2050A>T
ENST00000677190.1:n.2491A>T
ENST00000677239.1:c.1712A>T ENSP00000504087.1:p.Glu571Val
ENST00000677289.1:c.1603A>T ENSP00000504286.1:n.1603A>T
ENST00000677290.1:n.1937A>T
ENST00000677417.1:c.1712A>T ENSP00000503572.1:p.Glu571Val
ENST00000677422.1:c.*1147A>T ENSP00000503474.1:n.*1147A>T
ENST00000677476.1:c.1211A>T ENSP00000503789.1:p.Glu404Val
ENST00000677556.1:c.1319A>T ENSP00000504749.1:p.Glu440Val
ENST00000677803.1:c.1496A>T ENSP00000503702.1:p.Glu499Val
ENST00000677813.1:c.1712A>T ENSP00000504543.1:p.Glu571Val
ENST00000677814.1:c.1712A>T ENSP00000504848.1:p.Glu571Val
ENST00000677850.1:c.1712A>T ENSP00000504771.1:p.Glu571Val
ENST00000677928.1:c.1712A>T ENSP00000504198.1:p.Glu571Val
ENST00000677933.1:c.1712A>T ENSP00000503482.1:p.Glu571Val
ENST00000678081.1:c.1712A>T ENSP00000503194.1:p.Glu571Val
ENST00000678113.1:n.4638A>T
ENST00000678172.1:c.1712A>T ENSP00000503554.1:p.Glu571Val
ENST00000678182.1:c.1712A>T ENSP00000504594.1:p.Glu571Val
ENST00000678263.1:c.*1257A>T ENSP00000504172.1:n.*1257A>T
ENST00000678360.1:c.1712A>T ENSP00000503638.1:p.Glu571Val
ENST00000678741.1:c.1712A>T ENSP00000503395.1:p.Glu571Val
ENST00000678790.1:c.1712A>T ENSP00000503419.1:p.Glu571Val
ENST00000678877.1:c.1436A>T ENSP00000502889.1:p.Glu479Val
ENST00000679035.1:c.*1588A>T ENSP00000502854.1:n.*1588A>T
ENST00000680228.1:c.*1365A>T ENSP00000505574.1:n.*1365A>T
ENST00000401558.6:c.1712A>T ENSP00000384863.2:p.Glu571Val
ENST00000404992.6:c.1712A>T ENSP00000385942.2:p.Glu571Val
ENST00000406957.5:c.1712A>T ENSP00000385559.1:p.Glu571Val
ENST00000428210.5:c.*3461A>T ENSP00000407170.1:n.*3461A>T
ENST00000481073.5:n.1317A>T
NM_003400.3:c.1712A>T NP_003391.1:p.Glu571Val
XM_005264544.1:c.1667A>T XP_005264601.1:p.Glu556Val
XM_005264546.1:c.1319A>T XP_005264603.1:p.Glu440Val
XM_006712094.2:c.1712A>T XP_006712157.1:p.Glu571Val
XM_011533097.1:c.1712A>T XP_011531399.1:p.Glu571Val
XM_011533098.1:c.1712A>T XP_011531400.1:p.Glu571Val
XM_011533099.1:c.1514A>T XP_011531401.1:p.Glu505Val
XM_005264544.2:c.1667A>T XP_005264601.1:p.Glu556Val
XM_005264546.2:c.1319A>T XP_005264603.1:p.Glu440Val
XM_006712094.3:c.1712A>T XP_006712157.1:p.Glu571Val
XM_011533098.2:c.1712A>T XP_011531400.1:p.Glu571Val
XM_011533099.3:c.1514A>T XP_011531401.1:p.Glu505Val
XM_024453125.1:c.1712A>T XP_024308893.1:p.Glu571Val
XM_024453126.1:c.1712A>T XP_024308894.1:p.Glu571Val
XM_024453127.1:c.1319A>T XP_024308895.1:p.Glu440Val
NM_003400.4:c.1712A>T MANE Select NP_003391.1:p.Glu571Val