Canonical Allele Identifier: CA1624563013

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43523212C= , CM000668.2:g.43523212C= GRCh38
NC_000006.11:g.43490950C= , CM000668.1:g.43490950C= GRCh37
NC_000006.10:g.43598928C= NCBI36
NG_028283.1:g.11174C=
NG_028283.3:g.18511C=
NG_051658.1:g.57864G=

Transcript Alleles

HGVS Amino-acid change
ENST00000265351.12:c.*656G= (XPO5) MANE Select ENSP00000265351.7:n.*656G=
ENST00000607635.2:c.922+2164C= (POLR1C) ENSP00000496683.1:n.922+2164C=
ENST00000643341.1:c.922+2164C= (POLR1C) ENSP00000496018.1:n.922+2164C=
ENST00000643799.1:c.*17+1895C= (POLR1C) ENSP00000494529.1:n.*17+1895C=
ENST00000646433.1:c.922+2164C= (POLR1C) ENSP00000494368.1:n.922+2164C=
ENST00000646700.1:c.922+2164C= (POLR1C) ENSP00000495521.1:n.922+2164C=
ENST00000265351.11:c.*656G= (XPO5) ENSP00000265351.7:n.*656G=
ENST00000304004.7:c.922+2164C= (POLR1C) ENSP00000307212.3:n.922+2164C=
ENST00000455854.2:n.2754G= (XPO5)
NM_020750.2:c.*656G= (XPO5) NP_065801.1:n.*656G=
XM_005249491.1:c.922+2164C= (POLR1C) XP_005249548.1:n.922+2164C=
XM_011515000.1:c.922+2164C= (POLR1C) XP_011513302.1:n.922+2164C=
NM_001318876.1:c.922+2164C= (POLR1C) NP_001305805.1:n.922+2164C=
NM_001363658.1:c.922+2164C= (POLR1C) NP_001350587.1:n.922+2164C=
NR_144392.1:n.4620G= (XPO5)
NM_020750.3:c.*656G= (XPO5) MANE Select NP_065801.1:n.*656G=
NM_001363658.2:c.922+2164C= (POLR1C) NP_001350587.1:n.922+2164C=
NM_001318876.2:c.922+2164C= (POLR1C) NP_001305805.1:n.922+2164C=
NR_144392.2:n.4583G= (XPO5)