Canonical Allele Identifier: CA429445011

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145155925T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398358T>A , CM000664.2:g.144398358T>A	GRCh38
NC_000002.11:g.145155925T>A , CM000664.1:g.145155925T>A	GRCh37
NC_000002.10:g.144872395T>A	NCBI36
NG_016431.1:g.127034A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2678A>T	ENSP00000508434.1:n.*2678A>T
ENST00000440875.6:c.2052A>T	ENSP00000475553.3:p.Ala684=
ENST00000627532.3:c.2829A>T MANE Select	ENSP00000487174.1:p.Ala943=
ENST00000636026.2:c.2829A>T	ENSP00000490776.1:p.Ala943=
ENST00000636179.1:n.2798A>T
ENST00000636413.1:c.2493A>T	ENSP00000490508.1:p.Ala831=
ENST00000636471.1:c.2904A>T	ENSP00000490317.1:p.Ala968=
ENST00000636732.2:c.*2546A>T	ENSP00000490175.1:n.*2546A>T
ENST00000636820.1:n.2929A>T
ENST00000637045.1:c.2493A>T	ENSP00000490141.1:p.Ala831=
ENST00000637304.1:c.2493A>T	ENSP00000490872.1:p.Ala831=
ENST00000638007.1:c.2493A>T	ENSP00000490723.1:p.Ala831=
ENST00000638087.1:c.2493A>T	ENSP00000490673.1:p.Ala831=
ENST00000638128.1:c.2052A>T	ENSP00000490934.1:p.Ala684=
ENST00000675069.1:c.360A>T	ENSP00000502467.1:p.Ala120=
ENST00000303660.8:c.2826A>T	ENSP00000302501.4:p.Ala942=
ENST00000409487.7:c.2829A>T	ENSP00000386854.2:p.Ala943=
ENST00000419938.5:c.655+2841A>T	ENSP00000394777.2:n.655+2841A>T
ENST00000440875.5:c.1168-430A>T	ENSP00000475553.2:n.1168-430A>T
ENST00000539609.7:c.2757A>T	ENSP00000443792.2:p.Ala919=
ENST00000558170.6:c.2829A>T	ENSP00000454157.1:p.Ala943=
ENST00000627532.2:c.2829A>T	ENSP00000487174.1:p.Ala943=
NM_001171653.1:c.2757A>T	NP_001165124.1:p.Ala919=
NM_014795.3:c.2829A>T	NP_055610.1:p.Ala943=
XM_006712881.2:c.2829A>T	XP_006712944.1:p.Ala943=
XM_006712882.2:c.2829A>T	XP_006712945.1:p.Ala943=
XM_011512231.1:c.2820A>T	XP_011510533.1:p.Ala940=
XM_011512232.1:c.2808A>T	XP_011510534.1:p.Ala936=
NM_014795.4:c.2829A>T MANE Select	NP_055610.1:p.Ala943=
NM_001171653.2:c.2757A>T	NP_001165124.1:p.Ala919=