Canonical Allele Identifier: CA567152759

Gene: XPO5 POLR1C

Linked Data

• dbSNP Id: rs1243724820
• gnomAD v2: 6-43492548-C-T
• gnomAD v4: 6-43524810-C-T
• MyVariant Identifiers: chr6:g.43492548C>T (hg19) ; chr6:g.43524810C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43524810C>T , CM000668.2:g.43524810C>T	GRCh38
NC_000006.11:g.43492548C>T , CM000668.1:g.43492548C>T	GRCh37
NC_000006.10:g.43600526C>T	NCBI36
NG_028283.3:g.20109C>T
NG_051658.1:g.56266G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265351.12:c.3312+21G>A (XPO5) MANE Select	ENSP00000265351.7:n.3312+21G>A
ENST00000607635.2:c.922+3762C>T (POLR1C)	ENSP00000496683.1:n.922+3762C>T
ENST00000643341.1:c.922+3762C>T (POLR1C)	ENSP00000496018.1:n.922+3762C>T
ENST00000643799.1:c.*17+3493C>T (POLR1C)	ENSP00000494529.1:n.*17+3493C>T
ENST00000646433.1:c.922+3762C>T (POLR1C)	ENSP00000494368.1:n.922+3762C>T
ENST00000646700.1:c.922+3762C>T (POLR1C)	ENSP00000495521.1:n.922+3762C>T
ENST00000265351.11:c.3312+21G>A (XPO5)	ENSP00000265351.7:n.3312+21G>A
ENST00000304004.7:c.922+3762C>T (POLR1C)	ENSP00000307212.3:n.922+3762C>T
ENST00000455285.2:c.656+21G>A (XPO5)
ENST00000455854.2:n.1795+21G>A (XPO5)
ENST00000486936.2:c.499+21G>A (XPO5)
ENST00000488195.6:n.709+21G>A (XPO5)
NM_020750.2:c.3312+21G>A (XPO5)	NP_065801.1:n.3312+21G>A
XM_005249491.1:c.922+3762C>T (POLR1C)	XP_005249548.1:n.922+3762C>T
XM_011515000.1:c.922+3762C>T (POLR1C)	XP_011513302.1:n.922+3762C>T
NM_001318876.1:c.922+3762C>T (POLR1C)	NP_001305805.1:n.922+3762C>T
NM_001363658.1:c.922+3762C>T (POLR1C)	NP_001350587.1:n.922+3762C>T
NR_144392.1:n.3661+21G>A (XPO5)
NM_020750.3:c.3312+21G>A (XPO5) MANE Select	NP_065801.1:n.3312+21G>A
NM_001363658.2:c.922+3762C>T (POLR1C)	NP_001350587.1:n.922+3762C>T
NM_001318876.2:c.922+3762C>T (POLR1C)	NP_001305805.1:n.922+3762C>T
NR_144392.2:n.3624+21G>A (XPO5)