Canonical Allele Identifier: CA2580063843

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 2011486
• ClinVar RCV Id: RCV002829541

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398610dup , CM000664.2:g.144398610dup	GRCh38
NC_000002.11:g.145156177dup , CM000664.1:g.145156177dup	GRCh37
NC_000002.10:g.144872647dup	NCBI36
NG_016431.1:g.126782dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2426dup	ENSP00000508434.1:n.*2426dup
ENST00000440875.6:c.1800dup	ENSP00000475553.3:p.Leu601SerfsTer15
ENST00000627532.3:c.2577dup MANE Select	ENSP00000487174.1:p.Leu860SerfsTer15
ENST00000636026.2:c.2577dup	ENSP00000490776.1:p.Leu860SerfsTer15
ENST00000636179.1:n.2546dup
ENST00000636413.1:c.2241dup	ENSP00000490508.1:p.Leu748SerfsTer15
ENST00000636471.1:c.2652dup	ENSP00000490317.1:p.Leu885SerfsTer15
ENST00000636732.2:c.*2294dup	ENSP00000490175.1:n.*2294dup
ENST00000636820.1:n.2677dup
ENST00000637045.1:c.2241dup	ENSP00000490141.1:p.Leu748SerfsTer15
ENST00000637304.1:c.2241dup	ENSP00000490872.1:p.Leu748SerfsTer15
ENST00000638007.1:c.2241dup	ENSP00000490723.1:p.Leu748SerfsTer15
ENST00000638087.1:c.2241dup	ENSP00000490673.1:p.Leu748SerfsTer15
ENST00000638128.1:c.1800dup	ENSP00000490934.1:p.Leu601SerfsTer15
ENST00000675069.1:c.108dup	ENSP00000502467.1:p.Leu37SerfsTer15
ENST00000303660.8:c.2574dup	ENSP00000302501.4:p.Leu859SerfsTer15
ENST00000409487.7:c.2577dup	ENSP00000386854.2:p.Leu860SerfsTer15
ENST00000419938.5:c.655+2589dup	ENSP00000394777.2:n.655+2589dup
ENST00000440875.5:c.1168-682dup	ENSP00000475553.2:n.1168-682dup
ENST00000539609.7:c.2505dup	ENSP00000443792.2:p.Leu836SerfsTer15
ENST00000558170.6:c.2577dup	ENSP00000454157.1:p.Leu860SerfsTer15
ENST00000627532.2:c.2577dup	ENSP00000487174.1:p.Leu860SerfsTer15
NM_001171653.1:c.2505dup	NP_001165124.1:p.Leu836SerfsTer15
NM_014795.3:c.2577dup	NP_055610.1:p.Leu860SerfsTer15
XM_006712881.2:c.2577dup	XP_006712944.1:p.Leu860SerfsTer15
XM_006712882.2:c.2577dup	XP_006712945.1:p.Leu860SerfsTer15
XM_011512231.1:c.2568dup	XP_011510533.1:p.Leu857SerfsTer15
XM_011512232.1:c.2556dup	XP_011510534.1:p.Leu853SerfsTer15
NM_014795.4:c.2577dup MANE Select	NP_055610.1:p.Leu860SerfsTer15
NM_001171653.2:c.2505dup	NP_001165124.1:p.Leu836SerfsTer15