Canonical Allele Identifier: CA122595
Gene: ZEB1 HGNC NCBI
MyVariant.info:
Revel Score:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.31461211A>C , CM000672.2:g.31461211A>C GRCh38
NC_000010.10:g.31750140A>C , CM000672.1:g.31750140A>C GRCh37
NC_000010.9:g.31790146A>C NCBI36
NG_017048.1:g.147040A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000424869.6:c.233A>C MANE Select ENSP00000415961.2:p.Asn78Thr
ENST00000446923.7:c.182A>C ENSP00000391612.2:p.Asn61Thr
ENST00000320985.14:c.233A>C ENSP00000319248.9:p.Asn78Thr
ENST00000361642.9:c.233A>C ENSP00000354487.5:p.Asn78Thr
ENST00000424869.5:c.233A>C ENSP00000415961.1:p.Asn78Thr
ENST00000437844.6:c.*370A>C ENSP00000405958.3:n.*370A>C
ENST00000446923.6:c.182A>C ENSP00000391612.2:p.Asn61Thr
ENST00000488625.6:n.943A>C
ENST00000493835.5:n.658A>C
ENST00000542815.7:c.59-34568A>C ENSP00000444891.2:n.59-34568A>C
ENST00000542879.5:n.491A>C
ENST00000557827.5:n.377A>C
ENST00000558440.5:c.233A>C ENSP00000453970.1:p.Asn78Thr
ENST00000558655.5:n.327A>C
ENST00000558863.5:n.145-34568A>C
ENST00000559476.2:c.182A>C ENSP00000453674.1:p.Asn61Thr
ENST00000559496.5:n.872A>C
ENST00000559858.5:n.302A>C
ENST00000560196.5:n.825A>C
ENST00000560721.6:c.233A>C ENSP00000452787.1:p.Asn78Thr
ENST00000561061.5:n.411A>C
ENST00000561212.5:c.-422A>C ENSP00000453559.3:n.-422A>C
ENST00000561304.5:n.850A>C
ENST00000606161.1:n.337A>C
ENST00000606671.5:n.406A>C
NM_001128128.2:c.182A>C NP_001121600.1:p.Asn61Thr
NM_001174093.1:c.233A>C NP_001167564.1:p.Asn78Thr
NM_001174094.1:c.182A>C NP_001167565.1:p.Asn61Thr
NM_001174095.1:c.59-34568A>C NP_001167566.1:n.59-34568A>C
NM_001174096.1:c.233A>C NP_001167567.1:p.Asn78Thr
NM_030751.5:c.233A>C NP_110378.3:p.Asn78Thr
XM_005252576.1:c.-425A>C XP_005252633.1:n.-425A>C
XM_006717497.1:c.-425A>C XP_006717560.1:n.-425A>C
XM_006717498.1:c.-425A>C XP_006717561.1:n.-425A>C
XM_011519641.1:c.-425A>C XP_011517943.1:n.-425A>C
XM_011519642.1:c.-425A>C XP_011517944.1:n.-425A>C
XM_011519643.1:c.-425A>C XP_011517945.1:n.-425A>C
XM_011519644.1:c.-425A>C XP_011517946.1:n.-425A>C
XM_011519645.1:c.-425A>C XP_011517947.1:n.-425A>C
XM_011519646.1:c.-422A>C XP_011517948.1:n.-422A>C
XM_011519647.1:c.-422A>C XP_011517949.1:n.-422A>C
XM_011519648.1:c.-422A>C XP_011517950.1:n.-422A>C
NM_001323638.1:c.-425A>C NP_001310567.1:n.-425A>C
NM_001323641.1:c.-422A>C NP_001310570.1:n.-422A>C
NM_001323642.1:c.-425A>C NP_001310571.1:n.-425A>C
NM_001323643.1:c.-425A>C NP_001310572.1:n.-425A>C
NM_001323644.1:c.-395-34568A>C NP_001310573.1:n.-395-34568A>C
NM_001323645.1:c.-422A>C NP_001310574.1:n.-422A>C
NM_001323646.1:c.-425A>C NP_001310575.1:n.-425A>C
NM_001323647.1:c.-422A>C NP_001310576.1:n.-422A>C
NM_001323648.1:c.-362A>C NP_001310577.1:n.-362A>C
NM_001323649.1:c.-425A>C NP_001310578.1:n.-425A>C
NM_001323650.1:c.-422A>C NP_001310579.1:n.-422A>C
NM_001323651.1:c.-422A>C NP_001310580.1:n.-422A>C
NM_001323652.1:c.-422A>C NP_001310581.1:n.-422A>C
NM_001323653.1:c.-425A>C NP_001310582.1:n.-425A>C
NM_001323654.1:c.-422A>C NP_001310583.1:n.-422A>C
NM_001323655.1:c.-422A>C NP_001310584.1:n.-422A>C
NM_001323656.1:c.-422A>C NP_001310585.1:n.-422A>C
NM_001323657.1:c.-425A>C NP_001310586.1:n.-425A>C
NM_001323658.1:c.-389-34568A>C NP_001310587.1:n.-389-34568A>C
NM_001323659.1:c.-425A>C NP_001310588.1:n.-425A>C
NM_001323660.1:c.-422A>C NP_001310589.1:n.-422A>C
NM_001323661.1:c.-425A>C NP_001310590.1:n.-425A>C
NM_001323662.1:c.-425A>C NP_001310591.1:n.-425A>C
NM_001323663.1:c.-422A>C NP_001310592.1:n.-422A>C
NM_001323664.1:c.-425A>C NP_001310593.1:n.-425A>C
NM_001323665.1:c.-422A>C NP_001310594.1:n.-422A>C
NM_001323666.1:c.-362A>C NP_001310595.1:n.-362A>C
NM_001323671.1:c.-425A>C NP_001310600.1:n.-425A>C
NM_001323672.1:c.-425A>C NP_001310601.1:n.-425A>C
NM_001323673.1:c.-422A>C NP_001310602.1:n.-422A>C
NM_001323674.1:c.233A>C NP_001310603.1:p.Asn78Thr
NM_001323675.1:c.191A>C NP_001310604.1:p.Asn64Thr
NM_001323676.1:c.191A>C NP_001310605.1:p.Asn64Thr
NM_001323677.1:c.191A>C NP_001310606.1:p.Asn64Thr
NM_001323678.1:c.182A>C NP_001310607.1:p.Asn61Thr
XM_006717498.2:c.-425A>C XP_006717561.1:n.-425A>C
XM_011519643.2:c.-425A>C XP_011517945.1:n.-425A>C
XM_017016597.1:c.-425A>C XP_016872086.1:n.-425A>C
NM_001174093.2:c.233A>C NP_001167564.1:p.Asn78Thr
NM_001174094.2:c.182A>C NP_001167565.1:p.Asn61Thr
NM_001174095.2:c.59-34568A>C NP_001167566.1:n.59-34568A>C
NM_001323638.2:c.-425A>C NP_001310567.1:n.-425A>C
NM_001323641.2:c.-422A>C NP_001310570.1:n.-422A>C
NM_001323642.2:c.-425A>C NP_001310571.1:n.-425A>C
NM_001323643.2:c.-425A>C NP_001310572.1:n.-425A>C
NM_001323644.2:c.-395-34568A>C NP_001310573.1:n.-395-34568A>C
NM_001323645.2:c.-422A>C NP_001310574.1:n.-422A>C
NM_001323646.2:c.-425A>C NP_001310575.1:n.-425A>C
NM_001323647.2:c.-422A>C NP_001310576.1:n.-422A>C
NM_001323648.2:c.-362A>C NP_001310577.1:n.-362A>C
NM_001323649.2:c.-425A>C NP_001310578.1:n.-425A>C
NM_001323650.2:c.-422A>C NP_001310579.1:n.-422A>C
NM_001323651.2:c.-422A>C NP_001310580.1:n.-422A>C
NM_001323652.2:c.-422A>C NP_001310581.1:n.-422A>C
NM_001323653.2:c.-425A>C NP_001310582.1:n.-425A>C
NM_001323654.2:c.-422A>C NP_001310583.1:n.-422A>C
NM_001323655.2:c.-422A>C NP_001310584.1:n.-422A>C
NM_001323656.2:c.-422A>C NP_001310585.1:n.-422A>C
NM_001323657.2:c.-425A>C NP_001310586.1:n.-425A>C
NM_001323658.2:c.-389-34568A>C NP_001310587.1:n.-389-34568A>C
NM_001323659.2:c.-425A>C NP_001310588.1:n.-425A>C
NM_001323660.2:c.-422A>C NP_001310589.1:n.-422A>C
NM_001323661.2:c.-425A>C NP_001310590.1:n.-425A>C
NM_001323662.2:c.-425A>C NP_001310591.1:n.-425A>C
NM_001323663.2:c.-422A>C NP_001310592.1:n.-422A>C
NM_001323664.2:c.-425A>C NP_001310593.1:n.-425A>C
NM_001323665.2:c.-422A>C NP_001310594.1:n.-422A>C
NM_001323666.2:c.-362A>C NP_001310595.1:n.-362A>C
NM_001323671.2:c.-425A>C NP_001310600.1:n.-425A>C
NM_001323672.2:c.-425A>C NP_001310601.1:n.-425A>C
NM_001323673.2:c.-422A>C NP_001310602.1:n.-422A>C
NM_001323674.2:c.233A>C NP_001310603.1:p.Asn78Thr
NM_001323675.2:c.191A>C NP_001310604.1:p.Asn64Thr
NM_001323676.2:c.191A>C NP_001310605.1:p.Asn64Thr
NM_001323677.2:c.191A>C NP_001310606.1:p.Asn64Thr
NM_001323678.2:c.182A>C NP_001310607.1:p.Asn61Thr
NM_030751.6:c.233A>C NP_110378.3:p.Asn78Thr
NM_001128128.3:c.182A>C NP_001121600.1:p.Asn61Thr
NM_001174096.2:c.233A>C MANE Select NP_001167567.1:p.Asn78Thr