Canonical Allele Identifier: CA348708193

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 2786371
• ClinVar RCV Id: RCV003611807
• MyVariant Identifiers: chr2:g.145156278C>A (hg19) ; chr2:g.144398711C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398711C>A , CM000664.2:g.144398711C>A	GRCh38
NC_000002.11:g.145156278C>A , CM000664.1:g.145156278C>A	GRCh37
NC_000002.10:g.144872748C>A	NCBI36
NG_016431.1:g.126681G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2325G>T	ENSP00000508434.1:n.*2325G>T
ENST00000440875.6:c.1699G>T	ENSP00000475553.3:p.Glu567Ter
ENST00000627532.3:c.2476G>T MANE Select	ENSP00000487174.1:p.Glu826Ter
ENST00000636026.2:c.2476G>T	ENSP00000490776.1:p.Glu826Ter
ENST00000636179.1:n.2445G>T
ENST00000636413.1:c.2140G>T	ENSP00000490508.1:p.Glu714Ter
ENST00000636471.1:c.2551G>T	ENSP00000490317.1:p.Glu851Ter
ENST00000636732.2:c.*2193G>T	ENSP00000490175.1:n.*2193G>T
ENST00000636820.1:n.2576G>T
ENST00000637045.1:c.2140G>T	ENSP00000490141.1:p.Glu714Ter
ENST00000637304.1:c.2140G>T	ENSP00000490872.1:p.Glu714Ter
ENST00000638007.1:c.2140G>T	ENSP00000490723.1:p.Glu714Ter
ENST00000638087.1:c.2140G>T	ENSP00000490673.1:p.Glu714Ter
ENST00000638128.1:c.1699G>T	ENSP00000490934.1:p.Glu567Ter
ENST00000675069.1:c.7G>T	ENSP00000502467.1:p.Glu3Ter
ENST00000303660.8:c.2473G>T	ENSP00000302501.4:p.Glu825Ter
ENST00000409487.7:c.2476G>T	ENSP00000386854.2:p.Glu826Ter
ENST00000419938.5:c.655+2488G>T	ENSP00000394777.2:n.655+2488G>T
ENST00000440875.5:c.1168-783G>T	ENSP00000475553.2:n.1168-783G>T
ENST00000539609.7:c.2404G>T	ENSP00000443792.2:p.Glu802Ter
ENST00000558170.6:c.2476G>T	ENSP00000454157.1:p.Glu826Ter
ENST00000627532.2:c.2476G>T	ENSP00000487174.1:p.Glu826Ter
NM_001171653.1:c.2404G>T	NP_001165124.1:p.Glu802Ter
NM_014795.3:c.2476G>T	NP_055610.1:p.Glu826Ter
XM_006712881.2:c.2476G>T	XP_006712944.1:p.Glu826Ter
XM_006712882.2:c.2476G>T	XP_006712945.1:p.Glu826Ter
XM_011512231.1:c.2467G>T	XP_011510533.1:p.Glu823Ter
XM_011512232.1:c.2455G>T	XP_011510534.1:p.Glu819Ter
NM_014795.4:c.2476G>T MANE Select	NP_055610.1:p.Glu826Ter
NM_001171653.2:c.2404G>T	NP_001165124.1:p.Glu802Ter