Canonical Allele Identifier: CA12718123

Gene: XPO7

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.21963302C>A , CM000670.2:g.21963302C>A	GRCh38
NC_000008.10:g.21820813C>A , CM000670.1:g.21820813C>A	GRCh37
NC_000008.9:g.21876759C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252512.14:c.19-3555C>A MANE Select	ENSP00000252512.9:n.19-3555C>A
ENST00000252512.13:c.19-3555C>A	ENSP00000252512.9:n.19-3555C>A
ENST00000518017.1:n.214-3555C>A
ENST00000519769.5:n.30-3555C>A
ENST00000520754.1:n.172-847C>A
ENST00000521303.5:c.33-3555C>A
NM_015024.4:c.19-3555C>A	NP_055839.3:n.19-3555C>A
NM_001100161.1:c.19-3555C>A	NP_001093631.1:n.19-3555C>A
NM_001362802.1:c.19-3555C>A	NP_001349731.1:n.19-3555C>A
NR_156173.1:n.121-3555C>A
XM_024447108.1:c.27+2908C>A	XP_024302876.1:n.27+2908C>A
XM_024447109.1:c.27+2908C>A	XP_024302877.1:n.27+2908C>A
XM_024447110.1:c.27+2908C>A	XP_024302878.1:n.27+2908C>A
XR_002956623.1:n.1266+2908C>A
XR_002956624.1:n.42+2908C>A
NM_015024.5:c.19-3555C>A MANE Select	NP_055839.3:n.19-3555C>A
NM_001100161.2:c.19-3555C>A	NP_001093631.1:n.19-3555C>A
NM_001362802.2:c.19-3555C>A	NP_001349731.1:n.19-3555C>A
NR_156173.2:n.128-3555C>A