Canonical Allele Identifier: CA2586965031

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403937dup , CM000664.2:g.144403937dup	GRCh38
NC_000002.11:g.145161504dup , CM000664.1:g.145161504dup	GRCh37
NC_000002.10:g.144877974dup	NCBI36
NG_016431.1:g.121455dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*635dup	ENSP00000508434.1:n.*635dup
ENST00000440875.6:c.9dup	ENSP00000475553.3:p.His4ThrfsTer17
ENST00000627532.3:c.786dup MANE Select	ENSP00000487174.1:p.His263ThrfsTer17
ENST00000636026.2:c.786dup	ENSP00000490776.1:p.His263ThrfsTer17
ENST00000636179.1:n.755dup
ENST00000636413.1:c.450dup	ENSP00000490508.1:p.His151ThrfsTer17
ENST00000636471.1:c.786dup	ENSP00000490317.1:p.His263ThrfsTer17
ENST00000636732.2:c.*503dup	ENSP00000490175.1:n.*503dup
ENST00000636820.1:n.886dup
ENST00000637045.1:c.450dup	ENSP00000490141.1:p.His151ThrfsTer17
ENST00000637267.2:c.786dup	ENSP00000490293.2:p.His263ThrfsTer17
ENST00000637304.1:c.450dup	ENSP00000490872.1:p.His151ThrfsTer17
ENST00000638007.1:c.450dup	ENSP00000490723.1:p.His151ThrfsTer17
ENST00000638087.1:c.450dup	ENSP00000490673.1:p.His151ThrfsTer17
ENST00000638128.1:c.9dup	ENSP00000490934.1:p.His4ThrfsTer17
ENST00000675069.1:c.-133-5087dup	ENSP00000502467.1:n.-133-5087dup
ENST00000303660.8:c.783dup	ENSP00000302501.4:p.His262ThrfsTer17
ENST00000392861.6:c.870dup	ENSP00000376601.3:p.His291ThrfsTer17
ENST00000409487.7:c.786dup	ENSP00000386854.2:p.His263ThrfsTer17
ENST00000419938.5:c.525dup	ENSP00000394777.2:p.His176ThrfsTer17
ENST00000427902.5:c.873dup	ENSP00000395496.2:p.His292ThrfsTer17
ENST00000440875.5:c.771dup	ENSP00000475553.2:p.His258ThrfsTer17
ENST00000539609.7:c.714dup	ENSP00000443792.2:p.His239ThrfsTer17
ENST00000558170.6:c.786dup	ENSP00000454157.1:p.His263ThrfsTer17
ENST00000627532.2:c.786dup	ENSP00000487174.1:p.His263ThrfsTer17
NM_001171653.1:c.714dup	NP_001165124.1:p.His239ThrfsTer17
NM_014795.3:c.786dup	NP_055610.1:p.His263ThrfsTer17
XM_006712881.2:c.786dup	XP_006712944.1:p.His263ThrfsTer17
XM_006712882.2:c.786dup	XP_006712945.1:p.His263ThrfsTer17
XM_011512231.1:c.777dup	XP_011510533.1:p.His260ThrfsTer17
XM_011512232.1:c.765dup	XP_011510534.1:p.His256ThrfsTer17
NM_014795.4:c.786dup MANE Select	NP_055610.1:p.His263ThrfsTer17
NM_001171653.2:c.714dup	NP_001165124.1:p.His239ThrfsTer17