Canonical Allele Identifier: CA1624564359

Gene: XPO5 POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43524921G= , CM000668.2:g.43524921G=	GRCh38
NC_000006.11:g.43492659G= , CM000668.1:g.43492659G=	GRCh37
NC_000006.10:g.43600637G=	NCBI36
NG_028283.3:g.20220G=
NG_051658.1:g.56155C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265351.12:c.3222C= (XPO5) MANE Select	ENSP00000265351.7:p.Thr1074=
ENST00000607635.2:c.922+3873G= (POLR1C)	ENSP00000496683.1:n.922+3873G=
ENST00000643341.1:c.922+3873G= (POLR1C)	ENSP00000496018.1:n.922+3873G=
ENST00000643799.1:c.*17+3604G= (POLR1C)	ENSP00000494529.1:n.*17+3604G=
ENST00000646433.1:c.922+3873G= (POLR1C)	ENSP00000494368.1:n.922+3873G=
ENST00000646700.1:c.922+3873G= (POLR1C)	ENSP00000495521.1:n.922+3873G=
ENST00000265351.11:c.3222C= (XPO5)	ENSP00000265351.7:p.Thr1074=
ENST00000304004.7:c.922+3873G= (POLR1C)	ENSP00000307212.3:n.922+3873G=
ENST00000455285.2:c.566C= (XPO5)
ENST00000455854.2:n.1705C= (XPO5)
ENST00000486936.2:c.409C= (XPO5)
ENST00000488195.6:n.619C= (XPO5)
NM_020750.2:c.3222C= (XPO5)	NP_065801.1:p.Thr1074=
XM_005249491.1:c.922+3873G= (POLR1C)	XP_005249548.1:n.922+3873G=
XM_011515000.1:c.922+3873G= (POLR1C)	XP_011513302.1:n.922+3873G=
NM_001318876.1:c.922+3873G= (POLR1C)	NP_001305805.1:n.922+3873G=
NM_001363658.1:c.922+3873G= (POLR1C)	NP_001350587.1:n.922+3873G=
NR_144392.1:n.3571C= (XPO5)
NM_020750.3:c.3222C= (XPO5) MANE Select	NP_065801.1:p.Thr1074=
NM_001363658.2:c.922+3873G= (POLR1C)	NP_001350587.1:n.922+3873G=
NM_001318876.2:c.922+3873G= (POLR1C)	NP_001305805.1:n.922+3873G=
NR_144392.2:n.3534C= (XPO5)