Canonical Allele Identifier: CA138293747
Community Standard Title: NM_020750.3(XPO5):c.1313-298C>T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43556262G>A , CM000668.2:g.43556262G>A GRCh38
NC_000006.11:g.43523999G>A , CM000668.1:g.43523999G>A GRCh37
NC_000006.10:g.43631977G>A NCBI36
NG_028283.3:g.51561G>A
NG_051658.1:g.24814C>T

Transcript Alleles

HGVS Amino-acid Change
NM_020750.3:c.1313-298C>T (XPO5) MANE Select NP_065801.1:n.1313-298C>T
ENST00000265351.12:c.1313-298C>T (XPO5) MANE Select ENSP00000265351.7:n.1313-298C>T
NM_001318876.2:c.945+26991G>A (POLR1C) NP_001305805.1:n.945+26991G>A
NM_001363658.1:c.*43-5138G>A (POLR1C) NP_001350587.1:n.*43-5138G>A
NM_001363658.2:c.*43-5138G>A (POLR1C) NP_001350587.1:n.*43-5138G>A
NM_020750.2:c.1313-298C>T (XPO5) NP_065801.1:n.1313-298C>T
NR_144392.1:n.1524-298C>T (XPO5)
NR_144392.2:n.1487-298C>T (XPO5)
ENST00000265351.11:c.1313-298C>T (XPO5) ENSP00000265351.7:n.1313-298C>T
ENST00000424378.2:n.235-298C>T (XPO5)
ENST00000496341.6:c.298-298C>T (XPO5) ENSP00000424196.1:n.298-298C>T
ENST00000607635.2:c.*49-5138G>A (POLR1C) ENSP00000496683.1:n.*49-5138G>A
ENST00000643341.1:c.*43-5138G>A (POLR1C) ENSP00000496018.1:n.*43-5138G>A
ENST00000646433.1:c.923-5138G>A (POLR1C) ENSP00000494368.1:n.923-5138G>A