Canonical Allele Identifier: CA364287897

Gene: XPO5 POLR1C

Linked Data

• gnomAD v4: 6-43524611-C-T
• MyVariant Identifiers: chr6:g.43492349C>T (hg19) ; chr6:g.43524611C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43524611C>T , CM000668.2:g.43524611C>T	GRCh38
NC_000006.11:g.43492349C>T , CM000668.1:g.43492349C>T	GRCh37
NC_000006.10:g.43600327C>T	NCBI36
NG_028283.3:g.19910C>T
NG_051658.1:g.56465G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265351.12:c.3337G>A (XPO5) MANE Select	ENSP00000265351.7:p.Ala1113Thr
ENST00000607635.2:c.922+3563C>T (POLR1C)	ENSP00000496683.1:n.922+3563C>T
ENST00000643341.1:c.922+3563C>T (POLR1C)	ENSP00000496018.1:n.922+3563C>T
ENST00000643799.1:c.*17+3294C>T (POLR1C)	ENSP00000494529.1:n.*17+3294C>T
ENST00000646433.1:c.922+3563C>T (POLR1C)	ENSP00000494368.1:n.922+3563C>T
ENST00000646700.1:c.922+3563C>T (POLR1C)	ENSP00000495521.1:n.922+3563C>T
ENST00000265351.11:c.3337G>A (XPO5)	ENSP00000265351.7:p.Ala1113Thr
ENST00000304004.7:c.922+3563C>T (POLR1C)	ENSP00000307212.3:n.922+3563C>T
ENST00000455285.2:c.681G>A (XPO5)
ENST00000455854.2:n.1820G>A (XPO5)
ENST00000486936.2:c.524G>A (XPO5)
ENST00000488195.6:n.734G>A (XPO5)
NM_020750.2:c.3337G>A (XPO5)	NP_065801.1:p.Ala1113Thr
XM_005249491.1:c.922+3563C>T (POLR1C)	XP_005249548.1:n.922+3563C>T
XM_011515000.1:c.922+3563C>T (POLR1C)	XP_011513302.1:n.922+3563C>T
NM_001318876.1:c.922+3563C>T (POLR1C)	NP_001305805.1:n.922+3563C>T
NM_001363658.1:c.922+3563C>T (POLR1C)	NP_001350587.1:n.922+3563C>T
NR_144392.1:n.3686G>A (XPO5)
NM_020750.3:c.3337G>A (XPO5) MANE Select	NP_065801.1:p.Ala1113Thr
NM_001363658.2:c.922+3563C>T (POLR1C)	NP_001350587.1:n.922+3563C>T
NM_001318876.2:c.922+3563C>T (POLR1C)	NP_001305805.1:n.922+3563C>T
NR_144392.2:n.3649G>A (XPO5)