Canonical Allele Identifier: CA138289175

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43550032C>T , CM000668.2:g.43550032C>T GRCh38
NC_000006.11:g.43517769C>T , CM000668.1:g.43517769C>T GRCh37
NC_000006.10:g.43625747C>T NCBI36
NG_028283.3:g.45331C>T
NG_051658.1:g.31044G>A

Transcript Alleles

HGVS Amino-acid Change
NM_020750.3:c.1729-98G>A (XPO5) MANE Select NP_065801.1:n.1729-98G>A
ENST00000265351.12:c.1729-98G>A (XPO5) MANE Select ENSP00000265351.7:n.1729-98G>A
NM_001318876.2:c.945+20761C>T (POLR1C) NP_001305805.1:n.945+20761C>T
NM_001363658.1:c.923-936C>T (POLR1C) NP_001350587.1:n.923-936C>T
NM_001363658.2:c.923-936C>T (POLR1C) NP_001350587.1:n.923-936C>T
NM_020750.2:c.1729-98G>A (XPO5) NP_065801.1:n.1729-98G>A
NR_144392.1:n.1940-98G>A (XPO5)
NR_144392.2:n.1903-98G>A (XPO5)
ENST00000265351.11:c.1729-98G>A (XPO5) ENSP00000265351.7:n.1729-98G>A
ENST00000496341.6:c.714-98G>A (XPO5) ENSP00000424196.1:n.714-98G>A
ENST00000607635.2:c.*5-936C>T (POLR1C) ENSP00000496683.1:n.*5-936C>T
ENST00000643341.1:c.923-936C>T (POLR1C) ENSP00000496018.1:n.923-936C>T
ENST00000646433.1:c.923-11368C>T (POLR1C) ENSP00000494368.1:n.923-11368C>T
ENST00000646700.1:c.923-936C>T (POLR1C) ENSP00000495521.1:n.923-936C>T
XM_011515000.1:c.923-936C>T (POLR1C) XP_011513302.1:n.923-936C>T