Canonical Allele Identifier: CA364288132

Gene: XPO5 POLR1C

Linked Data

• MyVariant Identifiers: chr6:g.43492642A>G (hg19) ; chr6:g.43524904A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43524904A>G , CM000668.2:g.43524904A>G	GRCh38
NC_000006.11:g.43492642A>G , CM000668.1:g.43492642A>G	GRCh37
NC_000006.10:g.43600620A>G	NCBI36
NG_028283.3:g.20203A>G
NG_051658.1:g.56172T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265351.12:c.3239T>C (XPO5) MANE Select	ENSP00000265351.7:p.Leu1080Ser
ENST00000607635.2:c.922+3856A>G (POLR1C)	ENSP00000496683.1:n.922+3856A>G
ENST00000643341.1:c.922+3856A>G (POLR1C)	ENSP00000496018.1:n.922+3856A>G
ENST00000643799.1:c.*17+3587A>G (POLR1C)	ENSP00000494529.1:n.*17+3587A>G
ENST00000646433.1:c.922+3856A>G (POLR1C)	ENSP00000494368.1:n.922+3856A>G
ENST00000646700.1:c.922+3856A>G (POLR1C)	ENSP00000495521.1:n.922+3856A>G
ENST00000265351.11:c.3239T>C (XPO5)	ENSP00000265351.7:p.Leu1080Ser
ENST00000304004.7:c.922+3856A>G (POLR1C)	ENSP00000307212.3:n.922+3856A>G
ENST00000455285.2:c.583T>C (XPO5)
ENST00000455854.2:n.1722T>C (XPO5)
ENST00000486936.2:c.426T>C (XPO5)
ENST00000488195.6:n.636T>C (XPO5)
NM_020750.2:c.3239T>C (XPO5)	NP_065801.1:p.Leu1080Ser
XM_005249491.1:c.922+3856A>G (POLR1C)	XP_005249548.1:n.922+3856A>G
XM_011515000.1:c.922+3856A>G (POLR1C)	XP_011513302.1:n.922+3856A>G
NM_001318876.1:c.922+3856A>G (POLR1C)	NP_001305805.1:n.922+3856A>G
NM_001363658.1:c.922+3856A>G (POLR1C)	NP_001350587.1:n.922+3856A>G
NR_144392.1:n.3588T>C (XPO5)
NM_020750.3:c.3239T>C (XPO5) MANE Select	NP_065801.1:p.Leu1080Ser
NM_001363658.2:c.922+3856A>G (POLR1C)	NP_001350587.1:n.922+3856A>G
NM_001318876.2:c.922+3856A>G (POLR1C)	NP_001305805.1:n.922+3856A>G
NR_144392.2:n.3551T>C (XPO5)