Canonical Allele Identifier: CA2586970131

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399853dup , CM000664.2:g.144399853dup	GRCh38
NC_000002.11:g.145157420dup , CM000664.1:g.145157420dup	GRCh37
NC_000002.10:g.144873890dup	NCBI36
NG_016431.1:g.125542dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1186dup	ENSP00000508434.1:n.*1186dup
ENST00000440875.6:c.560dup	ENSP00000475553.3:p.Leu188PhefsTer9
ENST00000627532.3:c.1337dup MANE Select	ENSP00000487174.1:p.Leu447PhefsTer9
ENST00000636026.2:c.1337dup	ENSP00000490776.1:p.Leu447PhefsTer9
ENST00000636179.1:n.1306dup
ENST00000636413.1:c.1001dup	ENSP00000490508.1:p.Leu335PhefsTer9
ENST00000636471.1:c.1412dup	ENSP00000490317.1:p.Leu472PhefsTer9
ENST00000636732.2:c.*1054dup	ENSP00000490175.1:n.*1054dup
ENST00000636820.1:n.1437dup
ENST00000637045.1:c.1001dup	ENSP00000490141.1:p.Leu335PhefsTer9
ENST00000637267.2:c.1337dup	ENSP00000490293.2:p.Leu447PhefsTer9
ENST00000637304.1:c.1001dup	ENSP00000490872.1:p.Leu335PhefsTer9
ENST00000638007.1:c.1001dup	ENSP00000490723.1:p.Leu335PhefsTer9
ENST00000638087.1:c.1001dup	ENSP00000490673.1:p.Leu335PhefsTer9
ENST00000638128.1:c.560dup	ENSP00000490934.1:p.Leu188PhefsTer9
ENST00000675069.1:c.-133-1000dup	ENSP00000502467.1:n.-133-1000dup
ENST00000675145.1:n.1885dup
ENST00000303660.8:c.1334dup	ENSP00000302501.4:p.Leu446PhefsTer9
ENST00000409487.7:c.1337dup	ENSP00000386854.2:p.Leu447PhefsTer9
ENST00000419938.5:c.655+1349dup	ENSP00000394777.2:n.655+1349dup
ENST00000427902.5:c.1424dup	ENSP00000395496.2:p.Leu476PhefsTer9
ENST00000440875.5:c.1153+169dup	ENSP00000475553.2:n.1153+169dup
ENST00000539609.7:c.1265dup	ENSP00000443792.2:p.Leu423PhefsTer9
ENST00000558170.6:c.1337dup	ENSP00000454157.1:p.Leu447PhefsTer9
ENST00000627532.2:c.1337dup	ENSP00000487174.1:p.Leu447PhefsTer9
NM_001171653.1:c.1265dup	NP_001165124.1:p.Leu423PhefsTer9
NM_014795.3:c.1337dup	NP_055610.1:p.Leu447PhefsTer9
XM_006712881.2:c.1337dup	XP_006712944.1:p.Leu447PhefsTer9
XM_006712882.2:c.1337dup	XP_006712945.1:p.Leu447PhefsTer9
XM_011512231.1:c.1328dup	XP_011510533.1:p.Leu444PhefsTer9
XM_011512232.1:c.1316dup	XP_011510534.1:p.Leu440PhefsTer9
NM_014795.4:c.1337dup MANE Select	NP_055610.1:p.Leu447PhefsTer9
NM_001171653.2:c.1265dup	NP_001165124.1:p.Leu423PhefsTer9