Canonical Allele Identifier: CA138288766
Community Standard Title: NM_020750.3(XPO5):c.1860+128C>G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43549361G>C , CM000668.2:g.43549361G>C GRCh38
NC_000006.11:g.43517098G>C , CM000668.1:g.43517098G>C GRCh37
NC_000006.10:g.43625076G>C NCBI36
NG_028283.3:g.44660G>C
NG_051658.1:g.31715C>G

Transcript Alleles

HGVS Amino-acid Change
NM_020750.3:c.1860+128C>G (XPO5) MANE Select NP_065801.1:n.1860+128C>G
ENST00000265351.12:c.1860+128C>G (XPO5) MANE Select ENSP00000265351.7:n.1860+128C>G
NM_001318876.2:c.945+20090G>C (POLR1C) NP_001305805.1:n.945+20090G>C
NM_001363658.1:c.923-1607G>C (POLR1C) NP_001350587.1:n.923-1607G>C
NM_001363658.2:c.923-1607G>C (POLR1C) NP_001350587.1:n.923-1607G>C
NM_020750.2:c.1860+128C>G (XPO5) NP_065801.1:n.1860+128C>G
NR_144392.1:n.2071+128C>G (XPO5)
NR_144392.2:n.2034+128C>G (XPO5)
ENST00000265351.11:c.1860+128C>G (XPO5) ENSP00000265351.7:n.1860+128C>G
ENST00000607635.2:c.*5-1607G>C (POLR1C) ENSP00000496683.1:n.*5-1607G>C
ENST00000643341.1:c.923-1607G>C (POLR1C) ENSP00000496018.1:n.923-1607G>C
ENST00000646433.1:c.923-12039G>C (POLR1C) ENSP00000494368.1:n.923-12039G>C
ENST00000646700.1:c.923-1607G>C (POLR1C) ENSP00000495521.1:n.923-1607G>C
XM_011515000.1:c.923-1607G>C (POLR1C) XP_011513302.1:n.923-1607G>C