Canonical Allele Identifier: CA2586970070

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398342dup , CM000664.2:g.144398342dup	GRCh38
NC_000002.11:g.145155909dup , CM000664.1:g.145155909dup	GRCh37
NC_000002.10:g.144872379dup	NCBI36
NG_016431.1:g.127050dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2694dup	ENSP00000508434.1:n.*2694dup
ENST00000440875.6:c.2068dup	ENSP00000475553.3:p.Met690AsnfsTer19
ENST00000627532.3:c.2845dup MANE Select	ENSP00000487174.1:p.Met949AsnfsTer19
ENST00000636026.2:c.2845dup	ENSP00000490776.1:p.Met949AsnfsTer19
ENST00000636179.1:n.2814dup
ENST00000636413.1:c.2509dup	ENSP00000490508.1:p.Met837AsnfsTer19
ENST00000636471.1:c.2920dup	ENSP00000490317.1:p.Met974AsnfsTer19
ENST00000636732.2:c.*2562dup	ENSP00000490175.1:n.*2562dup
ENST00000636820.1:n.2945dup
ENST00000637045.1:c.2509dup	ENSP00000490141.1:p.Met837AsnfsTer19
ENST00000637304.1:c.2509dup	ENSP00000490872.1:p.Met837AsnfsTer19
ENST00000638007.1:c.2509dup	ENSP00000490723.1:p.Met837AsnfsTer19
ENST00000638087.1:c.2509dup	ENSP00000490673.1:p.Met837AsnfsTer19
ENST00000638128.1:c.2068dup	ENSP00000490934.1:p.Met690AsnfsTer19
ENST00000675069.1:c.376dup	ENSP00000502467.1:p.Met126AsnfsTer19
ENST00000303660.8:c.2842dup	ENSP00000302501.4:p.Met948AsnfsTer19
ENST00000409487.7:c.2845dup	ENSP00000386854.2:p.Met949AsnfsTer19
ENST00000419938.5:c.655+2857dup	ENSP00000394777.2:n.655+2857dup
ENST00000440875.5:c.1168-414dup	ENSP00000475553.2:n.1168-414dup
ENST00000539609.7:c.2773dup	ENSP00000443792.2:p.Met925AsnfsTer19
ENST00000558170.6:c.2845dup	ENSP00000454157.1:p.Met949AsnfsTer19
ENST00000627532.2:c.2845dup	ENSP00000487174.1:p.Met949AsnfsTer19
NM_001171653.1:c.2773dup	NP_001165124.1:p.Met925AsnfsTer19
NM_014795.3:c.2845dup	NP_055610.1:p.Met949AsnfsTer19
XM_006712881.2:c.2845dup	XP_006712944.1:p.Met949AsnfsTer19
XM_006712882.2:c.2845dup	XP_006712945.1:p.Met949AsnfsTer19
XM_011512231.1:c.2836dup	XP_011510533.1:p.Met946AsnfsTer19
XM_011512232.1:c.2824dup	XP_011510534.1:p.Met942AsnfsTer19
NM_014795.4:c.2845dup MANE Select	NP_055610.1:p.Met949AsnfsTer19
NM_001171653.2:c.2773dup	NP_001165124.1:p.Met925AsnfsTer19