Canonical Allele Identifier: CA351572

Gene: FUBP1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77956666C>T , CM000663.2:g.77956666C>T	GRCh38
NC_000001.10:g.78422351C>T , CM000663.1:g.78422351C>T	GRCh37
NC_000001.9:g.78194939C>T	NCBI36
NG_033243.2:g.27428G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421641.2:c.1671G>A	ENSP00000402630.2:p.Trp557Ter
ENST00000703586.1:c.1608G>A	ENSP00000515388.1:p.Trp536Ter
ENST00000370768.7:c.1611G>A MANE Select	ENSP00000359804.2:p.Trp537Ter
ENST00000294623.8:c.1608G>A	ENSP00000294623.4:p.Trp536Ter
ENST00000370767.5:c.1611G>A	ENSP00000359803.1:p.Trp537Ter
ENST00000370768.6:c.1611G>A	ENSP00000359804.2:p.Trp537Ter
ENST00000470287.1:n.557G>A
NM_001303433.1:c.1674G>A	NP_001290362.1:p.Trp558Ter
NM_003902.4:c.1611G>A	NP_003893.2:p.Trp537Ter
NR_130152.1:n.1809G>A
XM_011542391.1:c.1674G>A	XP_011540693.1:p.Trp558Ter
XM_011542392.1:c.1671G>A	XP_011540694.1:p.Trp557Ter
XM_011542393.1:c.1611G>A	XP_011540695.1:p.Trp537Ter
XM_011542394.1:c.1608G>A	XP_011540696.1:p.Trp536Ter
XM_011542395.1:c.1674G>A	XP_011540697.1:p.Trp558Ter
XR_946790.1:n.1779G>A
XR_946791.1:n.1870G>A
XR_946792.1:n.1870G>A
XR_946793.1:n.1779G>A
NR_146539.1:n.1809G>A
NR_146540.1:n.1812G>A
XM_011542391.3:c.1674G>A	XP_011540693.1:p.Trp558Ter
XM_011542392.2:c.1671G>A	XP_011540694.1:p.Trp557Ter
XM_011542393.3:c.1611G>A	XP_011540695.1:p.Trp537Ter
XM_017002739.1:c.1674G>A	XP_016858228.1:p.Trp558Ter
XM_017002740.2:c.1674G>A	XP_016858229.1:p.Trp558Ter
XM_017002742.1:c.1671G>A	XP_016858231.1:p.Trp557Ter
XM_017002743.2:c.1608G>A	XP_016858232.1:p.Trp536Ter
XM_017002744.2:c.1608G>A	XP_016858233.1:p.Trp536Ter
XM_024450628.1:c.1608G>A	XP_024306396.1:p.Trp536Ter
XR_001737514.2:n.1784G>A
XR_001737515.2:n.1784G>A
XR_001737516.2:n.1784G>A
XR_001737517.2:n.1784G>A
XR_001737518.2:n.1784G>A
XR_001737519.2:n.1784G>A
XR_001737520.1:n.1777G>A
XR_001737521.1:n.1875G>A
XR_001737522.2:n.1683G>A
XR_001737524.2:n.1734G>A
XR_946790.3:n.1784G>A
XR_946791.2:n.1875G>A
NR_130152.2:n.1676G>A
NR_146539.2:n.1676G>A
NR_146540.2:n.1679G>A
NM_001303433.2:c.1674G>A	NP_001290362.1:p.Trp558Ter
NM_001376055.1:c.1671G>A	NP_001362984.1:p.Trp557Ter
NM_001376056.1:c.1608G>A	NP_001362985.1:p.Trp536Ter
NM_001376057.1:c.1608G>A	NP_001362986.1:p.Trp536Ter
NM_003902.5:c.1611G>A MANE Select	NP_003893.2:p.Trp537Ter
NR_164755.1:n.1679G>A
NR_164756.1:n.1676G>A