Canonical Allele Identifier: CA2586970090

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398838dup , CM000664.2:g.144398838dup	GRCh38
NC_000002.11:g.145156405dup , CM000664.1:g.145156405dup	GRCh37
NC_000002.10:g.144872875dup	NCBI36
NG_016431.1:g.126555dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2199dup	ENSP00000508434.1:n.*2199dup
ENST00000440875.6:c.1573dup	ENSP00000475553.3:p.Ser525PhefsTer11
ENST00000627532.3:c.2350dup MANE Select	ENSP00000487174.1:p.Ser784PhefsTer11
ENST00000636026.2:c.2350dup	ENSP00000490776.1:p.Ser784PhefsTer11
ENST00000636179.1:n.2319dup
ENST00000636413.1:c.2014dup	ENSP00000490508.1:p.Ser672PhefsTer11
ENST00000636471.1:c.2425dup	ENSP00000490317.1:p.Ser809PhefsTer11
ENST00000636732.2:c.*2067dup	ENSP00000490175.1:n.*2067dup
ENST00000636820.1:n.2450dup
ENST00000637045.1:c.2014dup	ENSP00000490141.1:p.Ser672PhefsTer11
ENST00000637304.1:c.2014dup	ENSP00000490872.1:p.Ser672PhefsTer11
ENST00000638007.1:c.2014dup	ENSP00000490723.1:p.Ser672PhefsTer11
ENST00000638087.1:c.2014dup	ENSP00000490673.1:p.Ser672PhefsTer11
ENST00000638128.1:c.1573dup	ENSP00000490934.1:p.Ser525PhefsTer11
ENST00000675069.1:c.-120dup	ENSP00000502467.1:n.-120dup
ENST00000675145.1:n.2898dup
ENST00000303660.8:c.2347dup	ENSP00000302501.4:p.Ser783PhefsTer11
ENST00000409487.7:c.2350dup	ENSP00000386854.2:p.Ser784PhefsTer11
ENST00000419938.5:c.655+2362dup	ENSP00000394777.2:n.655+2362dup
ENST00000440875.5:c.1167+700dup	ENSP00000475553.2:n.1167+700dup
ENST00000539609.7:c.2278dup	ENSP00000443792.2:p.Ser760PhefsTer11
ENST00000558170.6:c.2350dup	ENSP00000454157.1:p.Ser784PhefsTer11
ENST00000627532.2:c.2350dup	ENSP00000487174.1:p.Ser784PhefsTer11
NM_001171653.1:c.2278dup	NP_001165124.1:p.Ser760PhefsTer11
NM_014795.3:c.2350dup	NP_055610.1:p.Ser784PhefsTer11
XM_006712881.2:c.2350dup	XP_006712944.1:p.Ser784PhefsTer11
XM_006712882.2:c.2350dup	XP_006712945.1:p.Ser784PhefsTer11
XM_011512231.1:c.2341dup	XP_011510533.1:p.Ser781PhefsTer11
XM_011512232.1:c.2329dup	XP_011510534.1:p.Ser777PhefsTer11
NM_014795.4:c.2350dup MANE Select	NP_055610.1:p.Ser784PhefsTer11
NM_001171653.2:c.2278dup	NP_001165124.1:p.Ser760PhefsTer11