Canonical Allele Identifier: CA3826210
Community Standard Title: NM_020750.3(XPO5):c.2161-39del

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43546803del , CM000668.2:g.43546803del GRCh38
NC_000006.11:g.43514540del , CM000668.1:g.43514540del GRCh37
NC_000006.10:g.43622518del NCBI36
NG_028283.3:g.42102del
NG_051658.1:g.34285del

Transcript Alleles

HGVS Amino-acid Change
NM_020750.3:c.2161-39del (XPO5) MANE Select NP_065801.1:n.2161-39del
ENST00000265351.12:c.2161-39del (XPO5) MANE Select ENSP00000265351.7:n.2161-39del
NM_001318876.2:c.945+17532del (POLR1C) NP_001305805.1:n.945+17532del
NM_001363658.1:c.923-4165del (POLR1C) NP_001350587.1:n.923-4165del
NM_001363658.2:c.923-4165del (POLR1C) NP_001350587.1:n.923-4165del
NM_020750.2:c.2161-39del (XPO5) NP_065801.1:n.2161-39del
NR_144392.1:n.2510-39del (XPO5)
NR_144392.2:n.2473-39del (XPO5)
ENST00000265351.11:c.2161-39del (XPO5) ENSP00000265351.7:n.2161-39del
ENST00000398835.7:c.207-39del (XPO5)
ENST00000607635.2:c.*5-4165del (POLR1C) ENSP00000496683.1:n.*5-4165del
ENST00000612911.1:n.75-39del (XPO5)
ENST00000643341.1:c.923-4165del (POLR1C) ENSP00000496018.1:n.923-4165del
ENST00000646433.1:c.923-14597del (POLR1C) ENSP00000494368.1:n.923-14597del
ENST00000646700.1:c.923-4165del (POLR1C) ENSP00000495521.1:n.923-4165del
XM_011515000.1:c.923-4165del (POLR1C) XP_011513302.1:n.923-4165del