Canonical Allele Identifier: CA2739271217

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 2824357
• ClinVar RCV Id: RCV003612852

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389658_144389660dup , CM000664.2:g.144389658_144389660dup	GRCh38
NC_000002.11:g.145147225_145147227dup , CM000664.1:g.145147225_145147227dup	GRCh37
NC_000002.10:g.144863695_144863697dup	NCBI36
NG_016431.1:g.135733_135735dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3286_*3288dup	ENSP00000508434.1:n.*3286_*3288dup
ENST00000440875.6:c.2660_2662dup	ENSP00000475553.3:p.Asp887_Gly888insAsp
ENST00000627532.3:c.3437_3439dup MANE Select	ENSP00000487174.1:p.Asp1146_Gly1147insAsp
ENST00000636026.2:c.3325_3327dup	ENSP00000490776.1:p.Met1109_Ala1110insMet
ENST00000636179.1:n.3406_3408dup
ENST00000636413.1:c.3101_3103dup	ENSP00000490508.1:p.Asp1034_Gly1035insAsp
ENST00000636471.1:c.3512_3514dup	ENSP00000490317.1:p.Asp1171_Gly1172insAsp
ENST00000636732.2:c.*3154_*3156dup	ENSP00000490175.1:n.*3154_*3156dup
ENST00000636820.1:n.3537_3539dup
ENST00000637045.1:c.3101_3103dup	ENSP00000490141.1:p.Asp1034_Gly1035insAsp
ENST00000637304.1:c.3101_3103dup	ENSP00000490872.1:p.Asp1034_Gly1035insAsp
ENST00000638007.1:c.3101_3103dup	ENSP00000490723.1:p.Asp1034_Gly1035insAsp
ENST00000638087.1:c.3101_3103dup	ENSP00000490673.1:p.Asp1034_Gly1035insAsp
ENST00000638128.1:c.2660_2662dup	ENSP00000490934.1:p.Asp887_Gly888insAsp
ENST00000639389.1:c.151+6753_151+6755dup	ENSP00000492572.1:n.151+6753_151+6755dup
ENST00000647488.1:c.657_659dup	ENSP00000494820.1:n.657_659dup
ENST00000675069.1:c.968_970dup	ENSP00000502467.1:p.Asp323_Gly324insAsp
ENST00000303660.8:c.3434_3436dup	ENSP00000302501.4:p.Asp1145_Gly1146insAsp
ENST00000409487.7:c.3437_3439dup	ENSP00000386854.2:p.Asp1146_Gly1147insAsp
ENST00000419938.5:c.656-777_656-775dup	ENSP00000394777.2:n.656-777_656-775dup
ENST00000539609.7:c.3365_3367dup	ENSP00000443792.2:p.Asp1122_Gly1123insAsp
ENST00000558170.6:c.3437_3439dup	ENSP00000454157.1:p.Asp1146_Gly1147insAsp
ENST00000627532.2:c.3437_3439dup	ENSP00000487174.1:p.Asp1146_Gly1147insAsp
NM_001171653.1:c.3365_3367dup	NP_001165124.1:p.Asp1122_Gly1123insAsp
NM_014795.3:c.3437_3439dup	NP_055610.1:p.Asp1146_Gly1147insAsp
XM_006712881.2:c.3437_3439dup	XP_006712944.1:p.Asp1146_Gly1147insAsp
XM_006712882.2:c.3437_3439dup	XP_006712945.1:p.Asp1146_Gly1147insAsp
XM_011512231.1:c.3428_3430dup	XP_011510533.1:p.Asp1143_Gly1144insAsp
XM_011512232.1:c.3416_3418dup	XP_011510534.1:p.Asp1139_Gly1140insAsp
NM_014795.4:c.3437_3439dup MANE Select	NP_055610.1:p.Asp1146_Gly1147insAsp
NM_001171653.2:c.3365_3367dup	NP_001165124.1:p.Asp1122_Gly1123insAsp