Canonical Allele Identifier: CA16043448

Gene: ZEB1

Linked Data

• ClinVar Variation Id: 374184
• ClinVar RCV Id: RCV000415113 ; RCV000599440
• dbSNP Id: rs1057518956
• gnomAD v4: 10-31520308-C-T
• COSMIC: COSM3782534 ; COSM3782535
• MyVariant Identifiers: chr10:g.31809236C>T (hg19) ; chr10:g.31520308C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.31520308C>T , CM000672.2:g.31520308C>T	GRCh38
NC_000010.10:g.31809236C>T , CM000672.1:g.31809236C>T	GRCh37
NC_000010.9:g.31849242C>T	NCBI36
NG_017048.1:g.206136C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424869.6:c.976C>T MANE Select	ENSP00000415961.2:p.Arg326Ter
ENST00000446923.7:c.925C>T	ENSP00000391612.2:p.Arg309Ter
ENST00000320985.14:c.973C>T	ENSP00000319248.9:p.Arg325Ter
ENST00000361642.9:c.976C>T	ENSP00000354487.5:p.Arg326Ter
ENST00000437844.6:c.*1113C>T	ENSP00000405958.3:n.*1113C>T
ENST00000446923.6:c.925C>T	ENSP00000391612.2:p.Arg309Ter
ENST00000488625.6:n.1686C>T
ENST00000542815.7:c.772C>T	ENSP00000444891.2:p.Arg258Ter
ENST00000542879.5:n.1231C>T
ENST00000558440.5:c.751C>T	ENSP00000453970.1:p.Arg251Ter
ENST00000558655.5:n.1070C>T
ENST00000558863.5:n.852C>T
ENST00000559858.5:n.1042C>T
ENST00000560721.6:c.913C>T	ENSP00000452787.1:p.Arg305Ter
ENST00000561212.5:c.319C>T	ENSP00000453559.3:p.Arg107Ter
NM_001128128.2:c.925C>T	NP_001121600.1:p.Arg309Ter
NM_001174093.1:c.913C>T	NP_001167564.1:p.Arg305Ter
NM_001174094.1:c.922C>T	NP_001167565.1:p.Arg308Ter
NM_001174095.1:c.772C>T	NP_001167566.1:p.Arg258Ter
NM_001174096.1:c.976C>T	NP_001167567.1:p.Arg326Ter
NM_030751.5:c.973C>T	NP_110378.3:p.Arg325Ter
XM_005252576.1:c.319C>T	XP_005252633.1:p.Arg107Ter
XM_006717497.1:c.319C>T	XP_006717560.1:p.Arg107Ter
XM_006717498.1:c.319C>T	XP_006717561.1:p.Arg107Ter
XM_011519641.1:c.319C>T	XP_011517943.1:p.Arg107Ter
XM_011519642.1:c.319C>T	XP_011517944.1:p.Arg107Ter
XM_011519643.1:c.319C>T	XP_011517945.1:p.Arg107Ter
XM_011519644.1:c.319C>T	XP_011517946.1:p.Arg107Ter
XM_011519645.1:c.319C>T	XP_011517947.1:p.Arg107Ter
XM_011519646.1:c.319C>T	XP_011517948.1:p.Arg107Ter
XM_011519647.1:c.319C>T	XP_011517949.1:p.Arg107Ter
XM_011519648.1:c.319C>T	XP_011517950.1:p.Arg107Ter
NM_001323638.1:c.319C>T	NP_001310567.1:p.Arg107Ter
NM_001323641.1:c.319C>T	NP_001310570.1:p.Arg107Ter
NM_001323642.1:c.319C>T	NP_001310571.1:p.Arg107Ter
NM_001323643.1:c.319C>T	NP_001310572.1:p.Arg107Ter
NM_001323644.1:c.319C>T	NP_001310573.1:p.Arg107Ter
NM_001323645.1:c.319C>T	NP_001310574.1:p.Arg107Ter
NM_001323646.1:c.319C>T	NP_001310575.1:p.Arg107Ter
NM_001323647.1:c.319C>T	NP_001310576.1:p.Arg107Ter
NM_001323648.1:c.319C>T	NP_001310577.1:p.Arg107Ter
NM_001323649.1:c.319C>T	NP_001310578.1:p.Arg107Ter
NM_001323650.1:c.319C>T	NP_001310579.1:p.Arg107Ter
NM_001323651.1:c.319C>T	NP_001310580.1:p.Arg107Ter
NM_001323652.1:c.319C>T	NP_001310581.1:p.Arg107Ter
NM_001323653.1:c.319C>T	NP_001310582.1:p.Arg107Ter
NM_001323654.1:c.319C>T	NP_001310583.1:p.Arg107Ter
NM_001323655.1:c.319C>T	NP_001310584.1:p.Arg107Ter
NM_001323656.1:c.319C>T	NP_001310585.1:p.Arg107Ter
NM_001323657.1:c.319C>T	NP_001310586.1:p.Arg107Ter
NM_001323658.1:c.319C>T	NP_001310587.1:p.Arg107Ter
NM_001323659.1:c.319C>T	NP_001310588.1:p.Arg107Ter
NM_001323660.1:c.319C>T	NP_001310589.1:p.Arg107Ter
NM_001323661.1:c.319C>T	NP_001310590.1:p.Arg107Ter
NM_001323662.1:c.319C>T	NP_001310591.1:p.Arg107Ter
NM_001323663.1:c.319C>T	NP_001310592.1:p.Arg107Ter
NM_001323664.1:c.319C>T	NP_001310593.1:p.Arg107Ter
NM_001323665.1:c.319C>T	NP_001310594.1:p.Arg107Ter
NM_001323666.1:c.319C>T	NP_001310595.1:p.Arg107Ter
NM_001323671.1:c.319C>T	NP_001310600.1:p.Arg107Ter
NM_001323672.1:c.319C>T	NP_001310601.1:p.Arg107Ter
NM_001323673.1:c.319C>T	NP_001310602.1:p.Arg107Ter
NM_001323674.1:c.751C>T	NP_001310603.1:p.Arg251Ter
NM_001323675.1:c.709C>T	NP_001310604.1:p.Arg237Ter
NM_001323676.1:c.934C>T	NP_001310605.1:p.Arg312Ter
NM_001323677.1:c.931C>T	NP_001310606.1:p.Arg311Ter
NM_001323678.1:c.700C>T	NP_001310607.1:p.Arg234Ter
XM_006717498.2:c.319C>T	XP_006717561.1:p.Arg107Ter
XM_011519643.2:c.319C>T	XP_011517945.1:p.Arg107Ter
XM_017016597.1:c.319C>T	XP_016872086.1:p.Arg107Ter
NM_001174093.2:c.913C>T	NP_001167564.1:p.Arg305Ter
NM_001174094.2:c.922C>T	NP_001167565.1:p.Arg308Ter
NM_001174095.2:c.772C>T	NP_001167566.1:p.Arg258Ter
NM_001323638.2:c.319C>T	NP_001310567.1:p.Arg107Ter
NM_001323641.2:c.319C>T	NP_001310570.1:p.Arg107Ter
NM_001323642.2:c.319C>T	NP_001310571.1:p.Arg107Ter
NM_001323643.2:c.319C>T	NP_001310572.1:p.Arg107Ter
NM_001323644.2:c.319C>T	NP_001310573.1:p.Arg107Ter
NM_001323645.2:c.319C>T	NP_001310574.1:p.Arg107Ter
NM_001323646.2:c.319C>T	NP_001310575.1:p.Arg107Ter
NM_001323647.2:c.319C>T	NP_001310576.1:p.Arg107Ter
NM_001323648.2:c.319C>T	NP_001310577.1:p.Arg107Ter
NM_001323649.2:c.319C>T	NP_001310578.1:p.Arg107Ter
NM_001323650.2:c.319C>T	NP_001310579.1:p.Arg107Ter
NM_001323651.2:c.319C>T	NP_001310580.1:p.Arg107Ter
NM_001323652.2:c.319C>T	NP_001310581.1:p.Arg107Ter
NM_001323653.2:c.319C>T	NP_001310582.1:p.Arg107Ter
NM_001323654.2:c.319C>T	NP_001310583.1:p.Arg107Ter
NM_001323655.2:c.319C>T	NP_001310584.1:p.Arg107Ter
NM_001323656.2:c.319C>T	NP_001310585.1:p.Arg107Ter
NM_001323657.2:c.319C>T	NP_001310586.1:p.Arg107Ter
NM_001323658.2:c.319C>T	NP_001310587.1:p.Arg107Ter
NM_001323659.2:c.319C>T	NP_001310588.1:p.Arg107Ter
NM_001323660.2:c.319C>T	NP_001310589.1:p.Arg107Ter
NM_001323661.2:c.319C>T	NP_001310590.1:p.Arg107Ter
NM_001323662.2:c.319C>T	NP_001310591.1:p.Arg107Ter
NM_001323663.2:c.319C>T	NP_001310592.1:p.Arg107Ter
NM_001323664.2:c.319C>T	NP_001310593.1:p.Arg107Ter
NM_001323665.2:c.319C>T	NP_001310594.1:p.Arg107Ter
NM_001323666.2:c.319C>T	NP_001310595.1:p.Arg107Ter
NM_001323671.2:c.319C>T	NP_001310600.1:p.Arg107Ter
NM_001323672.2:c.319C>T	NP_001310601.1:p.Arg107Ter
NM_001323673.2:c.319C>T	NP_001310602.1:p.Arg107Ter
NM_001323674.2:c.751C>T	NP_001310603.1:p.Arg251Ter
NM_001323675.2:c.709C>T	NP_001310604.1:p.Arg237Ter
NM_001323676.2:c.934C>T	NP_001310605.1:p.Arg312Ter
NM_001323677.2:c.931C>T	NP_001310606.1:p.Arg311Ter
NM_001323678.2:c.700C>T	NP_001310607.1:p.Arg234Ter
NM_030751.6:c.973C>T	NP_110378.3:p.Arg325Ter
NM_001128128.3:c.925C>T	NP_001121600.1:p.Arg309Ter
NM_001174096.2:c.976C>T MANE Select	NP_001167567.1:p.Arg326Ter