Canonical Allele Identifier: CA429218629

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1903610
• ClinVar RCV Id: RCV002586484
• gnomAD v4: 2-144404087-G-A
• MyVariant Identifiers: chr2:g.145161654G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404087G>A , CM000664.2:g.144404087G>A	GRCh38
NC_000002.11:g.145161654G>A , CM000664.1:g.145161654G>A	GRCh37
NC_000002.10:g.144878124G>A	NCBI36
NG_016431.1:g.121305C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*485C>T	ENSP00000508434.1:n.*485C>T
ENST00000440875.6:c.-142C>T	ENSP00000475553.3:n.-142C>T
ENST00000627532.3:c.636C>T MANE Select	ENSP00000487174.1:p.Thr212=
ENST00000636026.2:c.636C>T	ENSP00000490776.1:p.Thr212=
ENST00000636179.1:n.605C>T
ENST00000636413.1:c.300C>T	ENSP00000490508.1:p.Thr100=
ENST00000636471.1:c.636C>T	ENSP00000490317.1:p.Thr212=
ENST00000636732.2:c.*353C>T	ENSP00000490175.1:n.*353C>T
ENST00000636820.1:n.736C>T
ENST00000637045.1:c.300C>T	ENSP00000490141.1:p.Thr100=
ENST00000637267.2:c.636C>T	ENSP00000490293.2:p.Thr212=
ENST00000637304.1:c.300C>T	ENSP00000490872.1:p.Thr100=
ENST00000638007.1:c.300C>T	ENSP00000490723.1:p.Thr100=
ENST00000638087.1:c.300C>T	ENSP00000490673.1:p.Thr100=
ENST00000638128.1:c.-142C>T	ENSP00000490934.1:n.-142C>T
ENST00000675069.1:c.-133-5237C>T	ENSP00000502467.1:n.-133-5237C>T
ENST00000303660.8:c.633C>T	ENSP00000302501.4:p.Thr211=
ENST00000392861.6:c.720C>T	ENSP00000376601.3:p.Thr240=
ENST00000409487.7:c.636C>T	ENSP00000386854.2:p.Thr212=
ENST00000419938.5:c.375C>T	ENSP00000394777.2:p.Thr125=
ENST00000427902.5:c.723C>T	ENSP00000395496.2:p.Thr241=
ENST00000440875.5:c.621C>T	ENSP00000475553.2:p.Thr207=
ENST00000497268.1:n.582C>T
ENST00000539609.7:c.564C>T	ENSP00000443792.2:p.Thr188=
ENST00000558170.6:c.636C>T	ENSP00000454157.1:p.Thr212=
ENST00000627532.2:c.636C>T	ENSP00000487174.1:p.Thr212=
NM_001171653.1:c.564C>T	NP_001165124.1:p.Thr188=
NM_014795.3:c.636C>T	NP_055610.1:p.Thr212=
XM_006712881.2:c.636C>T	XP_006712944.1:p.Thr212=
XM_006712882.2:c.636C>T	XP_006712945.1:p.Thr212=
XM_011512231.1:c.627C>T	XP_011510533.1:p.Thr209=
XM_011512232.1:c.615C>T	XP_011510534.1:p.Thr205=
NM_014795.4:c.636C>T MANE Select	NP_055610.1:p.Thr212=
NM_001171653.2:c.564C>T	NP_001165124.1:p.Thr188=