Canonical Allele Identifier: CA1294881242

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389544_144389547delinsCTCT , CM000664.2:g.144389544_144389547delinsCTCT	GRCh38
NC_000002.11:g.145147111_145147114delinsCTCT , CM000664.1:g.145147111_145147114delinsCTCT	GRCh37
NC_000002.10:g.144863581_144863584delinsCTCT	NCBI36
NG_016431.1:g.135845_135848delinsAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3398_*3401delinsAGAG	ENSP00000508434.1:n.*3398_*3401delinsAGAG
ENST00000440875.6:c.2772_2775delinsAGAG	ENSP00000475553.3:p.Glu924=
ENST00000627532.3:c.3549_3552delinsAGAG MANE Select	ENSP00000487174.1:p.Glu1183=
ENST00000636026.2:c.3437_3440delinsAGAG	ENSP00000490776.1:p.Lys1146=
ENST00000636179.1:n.3518_3521delinsAGAG
ENST00000636413.1:c.3213_3216delinsAGAG	ENSP00000490508.1:p.Glu1071=
ENST00000636471.1:c.3624_3627delinsAGAG	ENSP00000490317.1:p.Glu1208=
ENST00000636732.2:c.*3266_*3269delinsAGAG	ENSP00000490175.1:n.*3266_*3269delinsAGAG
ENST00000636820.1:n.3649_3652delinsAGAG
ENST00000637045.1:c.3213_3216delinsAGAG	ENSP00000490141.1:p.Glu1071=
ENST00000637304.1:c.3213_3216delinsAGAG	ENSP00000490872.1:p.Glu1071=
ENST00000638007.1:c.3213_3216delinsAGAG	ENSP00000490723.1:p.Glu1071=
ENST00000638087.1:c.3213_3216delinsAGAG	ENSP00000490673.1:p.Glu1071=
ENST00000638128.1:c.2772_2775delinsAGAG	ENSP00000490934.1:p.Glu924=
ENST00000639389.1:c.151+6865_151+6868delinsAGAG	ENSP00000492572.1:n.151+6865_151+6868delinsAGAG
ENST00000647488.1:c.769_772delinsAGAG	ENSP00000494820.1:n.769_772delinsAGAG
ENST00000675069.1:c.1080_1083delinsAGAG	ENSP00000502467.1:p.Glu360=
ENST00000303660.8:c.3546_3549delinsAGAG	ENSP00000302501.4:p.Glu1182=
ENST00000409487.7:c.3549_3552delinsAGAG	ENSP00000386854.2:p.Glu1183=
ENST00000419938.5:c.656-665_656-662delinsAGAG	ENSP00000394777.2:n.656-665_656-662delinsAGAG
ENST00000539609.7:c.3477_3480delinsAGAG	ENSP00000443792.2:p.Glu1159=
ENST00000558170.6:c.3549_3552delinsAGAG	ENSP00000454157.1:p.Glu1183=
ENST00000627532.2:c.3549_3552delinsAGAG	ENSP00000487174.1:p.Glu1183=
NM_001171653.1:c.3477_3480delinsAGAG	NP_001165124.1:p.Glu1159=
NM_014795.3:c.3549_3552delinsAGAG	NP_055610.1:p.Glu1183=
XM_006712881.2:c.3549_3552delinsAGAG	XP_006712944.1:p.Glu1183=
XM_006712882.2:c.3549_3552delinsAGAG	XP_006712945.1:p.Glu1183=
XM_011512231.1:c.3540_3543delinsAGAG	XP_011510533.1:p.Glu1180=
XM_011512232.1:c.3528_3531delinsAGAG	XP_011510534.1:p.Glu1176=
NM_014795.4:c.3549_3552delinsAGAG MANE Select	NP_055610.1:p.Glu1183=
NM_001171653.2:c.3477_3480delinsAGAG	NP_001165124.1:p.Glu1159=