Canonical Allele Identifier: CA429217602

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145154061C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396494C>T , CM000664.2:g.144396494C>T	GRCh38
NC_000002.11:g.145154061C>T , CM000664.1:g.145154061C>T	GRCh37
NC_000002.10:g.144870531C>T	NCBI36
NG_016431.1:g.128898G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2834G>A	ENSP00000508434.1:n.*2834G>A
ENST00000440875.6:c.2208G>A	ENSP00000475553.3:p.Glu736=
ENST00000627532.3:c.2985G>A MANE Select	ENSP00000487174.1:p.Glu995=
ENST00000636026.2:c.2985G>A	ENSP00000490776.1:p.Glu995=
ENST00000636179.1:n.2954G>A
ENST00000636413.1:c.2649G>A	ENSP00000490508.1:p.Glu883=
ENST00000636471.1:c.3060G>A	ENSP00000490317.1:p.Glu1020=
ENST00000636732.2:c.*2702G>A	ENSP00000490175.1:n.*2702G>A
ENST00000636820.1:n.3085G>A
ENST00000637045.1:c.2649G>A	ENSP00000490141.1:p.Glu883=
ENST00000637304.1:c.2649G>A	ENSP00000490872.1:p.Glu883=
ENST00000638007.1:c.2649G>A	ENSP00000490723.1:p.Glu883=
ENST00000638087.1:c.2649G>A	ENSP00000490673.1:p.Glu883=
ENST00000638128.1:c.2208G>A	ENSP00000490934.1:p.Glu736=
ENST00000639389.1:c.69G>A	ENSP00000492572.1:p.Glu23=
ENST00000647488.1:c.117G>A	ENSP00000494820.1:p.Glu39=
ENST00000675069.1:c.516G>A	ENSP00000502467.1:p.Glu172=
ENST00000303660.8:c.2982G>A	ENSP00000302501.4:p.Glu994=
ENST00000409487.7:c.2985G>A	ENSP00000386854.2:p.Glu995=
ENST00000419938.5:c.655+4705G>A	ENSP00000394777.2:n.655+4705G>A
ENST00000539609.7:c.2913G>A	ENSP00000443792.2:p.Glu971=
ENST00000558170.6:c.2985G>A	ENSP00000454157.1:p.Glu995=
ENST00000627532.2:c.2985G>A	ENSP00000487174.1:p.Glu995=
NM_001171653.1:c.2913G>A	NP_001165124.1:p.Glu971=
NM_014795.3:c.2985G>A	NP_055610.1:p.Glu995=
XM_006712881.2:c.2985G>A	XP_006712944.1:p.Glu995=
XM_006712882.2:c.2985G>A	XP_006712945.1:p.Glu995=
XM_011512231.1:c.2976G>A	XP_011510533.1:p.Glu992=
XM_011512232.1:c.2964G>A	XP_011510534.1:p.Glu988=
NM_014795.4:c.2985G>A MANE Select	NP_055610.1:p.Glu995=
NM_001171653.2:c.2913G>A	NP_001165124.1:p.Glu971=