Canonical Allele Identifier: CA376495163

Gene: ZEB1 ZEB1-AS1

Linked Data

• ClinVar Variation Id: 488897
• ClinVar RCV Id: RCV000579251 ; RCV003991031
• dbSNP Id: rs1554797626
• MyVariant Identifiers: chr10:g.31608166G>A (hg19) ; chr10:g.31319237G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.31319237G>A , CM000672.2:g.31319237G>A	GRCh38
NC_000010.10:g.31608166G>A , CM000672.1:g.31608166G>A	GRCh37
NC_000010.9:g.31648172G>A	NCBI36
NG_017048.1:g.5066G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424869.6:c.3G>A (ZEB1) MANE Select	ENSP00000415961.2:p.Met1Ile
ENST00000320985.14:c.3G>A (ZEB1)	ENSP00000319248.9:p.Met1Ile
ENST00000361642.9:c.3G>A (ZEB1)	ENSP00000354487.5:p.Met1Ile
ENST00000424869.5:c.3G>A (ZEB1)	ENSP00000415961.1:p.Met1Ile
ENST00000437844.6:c.3G>A (ZEB1)	ENSP00000405958.3:p.Met1Ile
ENST00000488625.6:n.307+104G>A (ZEB1)
ENST00000542815.7:c.3G>A (ZEB1)	ENSP00000444891.2:p.Met1Ile
ENST00000542879.5:n.316+104G>A (ZEB1)
ENST00000558440.5:c.3G>A (ZEB1)	ENSP00000453970.1:p.Met1Ile
ENST00000559858.5:n.26G>A (ZEB1)
ENST00000560196.5:n.351+104G>A (ZEB1)
ENST00000560721.6:c.3G>A (ZEB1)	ENSP00000452787.1:p.Met1Ile
ENST00000561304.5:n.297+104G>A (ZEB1)
NM_001174093.1:c.3G>A (ZEB1)	NP_001167564.1:p.Met1Ile
NM_001174095.1:c.3G>A (ZEB1)	NP_001167566.1:p.Met1Ile
NM_001174096.1:c.3G>A (ZEB1)	NP_001167567.1:p.Met1Ile
NM_030751.5:c.3G>A (ZEB1)	NP_110378.3:p.Met1Ile
XM_005252576.1:c.-798G>A (ZEB1)	XP_005252633.1:n.-798G>A
XM_006717498.1:c.-1116G>A (ZEB1)	XP_006717561.1:n.-1116G>A
XM_011519644.1:c.-899+104G>A (ZEB1)	XP_011517946.1:n.-899+104G>A
XM_011519645.1:c.-978+104G>A (ZEB1)	XP_011517947.1:n.-978+104G>A
XM_011519648.1:c.-1030G>A (ZEB1)	XP_011517950.1:n.-1030G>A
XR_930800.1:n.414+1046C>T
XR_930801.1:n.414+1046C>T
NM_001323638.1:c.-1061+104G>A (ZEB1)	NP_001310567.1:n.-1061+104G>A
NM_001323641.1:c.-597+104G>A (ZEB1)	NP_001310570.1:n.-597+104G>A
NM_001323642.1:c.-899+104G>A (ZEB1)	NP_001310571.1:n.-899+104G>A
NM_001323643.1:c.-721+104G>A (ZEB1)	NP_001310572.1:n.-721+104G>A
NM_001323644.1:c.-396+104G>A (ZEB1)	NP_001310573.1:n.-396+104G>A
NM_001323645.1:c.-740+104G>A (ZEB1)	NP_001310574.1:n.-740+104G>A
NM_001323646.1:c.-978+104G>A (ZEB1)	NP_001310575.1:n.-978+104G>A
NM_001323647.1:c.-795G>A (ZEB1)	NP_001310576.1:n.-795G>A
NM_001323648.1:c.-735G>A (ZEB1)	NP_001310577.1:n.-735G>A
NM_001323649.1:c.-798G>A (ZEB1)	NP_001310578.1:n.-798G>A
NM_001323650.1:c.-1030G>A (ZEB1)	NP_001310579.1:n.-1030G>A
NM_001323651.1:c.-698G>A (ZEB1)	NP_001310580.1:n.-698G>A
NM_001323652.1:c.-847G>A (ZEB1)	NP_001310581.1:n.-847G>A
NM_001323653.1:c.-954G>A (ZEB1)	NP_001310582.1:n.-954G>A
NM_001323654.1:c.-841G>A (ZEB1)	NP_001310583.1:n.-841G>A
NM_001323655.1:c.-951G>A (ZEB1)	NP_001310584.1:n.-951G>A
NM_001323674.1:c.3G>A (ZEB1)	NP_001310603.1:p.Met1Ile
NR_148975.1:n.166-697C>T (ZEB1-AS1)
NR_148976.1:n.367+278C>T (ZEB1-AS1)
XM_006717498.2:c.-1116G>A (ZEB1)	XP_006717561.1:n.-1116G>A
XM_017016597.1:c.-1033G>A (ZEB1)	XP_016872086.1:n.-1033G>A
NM_001174093.2:c.3G>A (ZEB1)	NP_001167564.1:p.Met1Ile
NM_001174095.2:c.3G>A (ZEB1)	NP_001167566.1:p.Met1Ile
NM_001323638.2:c.-1061+104G>A (ZEB1)	NP_001310567.1:n.-1061+104G>A
NM_001323641.2:c.-597+104G>A (ZEB1)	NP_001310570.1:n.-597+104G>A
NM_001323642.2:c.-899+104G>A (ZEB1)	NP_001310571.1:n.-899+104G>A
NM_001323643.2:c.-721+104G>A (ZEB1)	NP_001310572.1:n.-721+104G>A
NM_001323644.2:c.-396+104G>A (ZEB1)	NP_001310573.1:n.-396+104G>A
NM_001323645.2:c.-740+104G>A (ZEB1)	NP_001310574.1:n.-740+104G>A
NM_001323646.2:c.-978+104G>A (ZEB1)	NP_001310575.1:n.-978+104G>A
NM_001323647.2:c.-795G>A (ZEB1)	NP_001310576.1:n.-795G>A
NM_001323648.2:c.-735G>A (ZEB1)	NP_001310577.1:n.-735G>A
NM_001323649.2:c.-798G>A (ZEB1)	NP_001310578.1:n.-798G>A
NM_001323650.2:c.-1030G>A (ZEB1)	NP_001310579.1:n.-1030G>A
NM_001323651.2:c.-698G>A (ZEB1)	NP_001310580.1:n.-698G>A
NM_001323652.2:c.-847G>A (ZEB1)	NP_001310581.1:n.-847G>A
NM_001323653.2:c.-954G>A (ZEB1)	NP_001310582.1:n.-954G>A
NM_001323654.2:c.-841G>A (ZEB1)	NP_001310583.1:n.-841G>A
NM_001323655.2:c.-951G>A (ZEB1)	NP_001310584.1:n.-951G>A
NM_001323674.2:c.3G>A (ZEB1)	NP_001310603.1:p.Met1Ile
NM_030751.6:c.3G>A (ZEB1)	NP_110378.3:p.Met1Ile
NM_001174096.2:c.3G>A (ZEB1) MANE Select	NP_001167567.1:p.Met1Ile