Canonical Allele Identifier: CA2580063848

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1802548
• ClinVar RCV Id: RCV002465387

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398831dup , CM000664.2:g.144398831dup	GRCh38
NC_000002.11:g.145156398dup , CM000664.1:g.145156398dup	GRCh37
NC_000002.10:g.144872868dup	NCBI36
NG_016431.1:g.126562dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2206dup	ENSP00000508434.1:n.*2206dup
ENST00000440875.6:c.1580dup	ENSP00000475553.3:p.Leu527PhefsTer9
ENST00000627532.3:c.2357dup MANE Select	ENSP00000487174.1:p.Leu786PhefsTer9
ENST00000636026.2:c.2357dup	ENSP00000490776.1:p.Leu786PhefsTer9
ENST00000636179.1:n.2326dup
ENST00000636413.1:c.2021dup	ENSP00000490508.1:p.Leu674PhefsTer9
ENST00000636471.1:c.2432dup	ENSP00000490317.1:p.Leu811PhefsTer9
ENST00000636732.2:c.*2074dup	ENSP00000490175.1:n.*2074dup
ENST00000636820.1:n.2457dup
ENST00000637045.1:c.2021dup	ENSP00000490141.1:p.Leu674PhefsTer9
ENST00000637304.1:c.2021dup	ENSP00000490872.1:p.Leu674PhefsTer9
ENST00000638007.1:c.2021dup	ENSP00000490723.1:p.Leu674PhefsTer9
ENST00000638087.1:c.2021dup	ENSP00000490673.1:p.Leu674PhefsTer9
ENST00000638128.1:c.1580dup	ENSP00000490934.1:p.Leu527PhefsTer9
ENST00000675069.1:c.-113dup	ENSP00000502467.1:n.-113dup
ENST00000675145.1:n.2905dup
ENST00000303660.8:c.2354dup	ENSP00000302501.4:p.Leu785PhefsTer9
ENST00000409487.7:c.2357dup	ENSP00000386854.2:p.Leu786PhefsTer9
ENST00000419938.5:c.655+2369dup	ENSP00000394777.2:n.655+2369dup
ENST00000440875.5:c.1167+707dup	ENSP00000475553.2:n.1167+707dup
ENST00000539609.7:c.2285dup	ENSP00000443792.2:p.Leu762PhefsTer9
ENST00000558170.6:c.2357dup	ENSP00000454157.1:p.Leu786PhefsTer9
ENST00000627532.2:c.2357dup	ENSP00000487174.1:p.Leu786PhefsTer9
NM_001171653.1:c.2285dup	NP_001165124.1:p.Leu762PhefsTer9
NM_014795.3:c.2357dup	NP_055610.1:p.Leu786PhefsTer9
XM_006712881.2:c.2357dup	XP_006712944.1:p.Leu786PhefsTer9
XM_006712882.2:c.2357dup	XP_006712945.1:p.Leu786PhefsTer9
XM_011512231.1:c.2348dup	XP_011510533.1:p.Leu783PhefsTer9
XM_011512232.1:c.2336dup	XP_011510534.1:p.Leu779PhefsTer9
NM_014795.4:c.2357dup MANE Select	NP_055610.1:p.Leu786PhefsTer9
NM_001171653.2:c.2285dup	NP_001165124.1:p.Leu762PhefsTer9