Canonical Allele Identifier: CA2586965039

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 2687502
• ClinVar RCV Id: RCV003484252

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404072_144404075dup , CM000664.2:g.144404072_144404075dup	GRCh38
NC_000002.11:g.145161639_145161642dup , CM000664.1:g.145161639_145161642dup	GRCh37
NC_000002.10:g.144878109_144878112dup	NCBI36
NG_016431.1:g.121319_121322dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*499_*502dup	ENSP00000508434.1:n.*499_*502dup
ENST00000440875.6:c.-128_-125dup	ENSP00000475553.3:n.-128_-125dup
ENST00000627532.3:c.650_653dup MANE Select	ENSP00000487174.1:p.Gly219ProfsTer21
ENST00000636026.2:c.650_653dup	ENSP00000490776.1:p.Gly219ProfsTer21
ENST00000636179.1:n.619_622dup
ENST00000636413.1:c.314_317dup	ENSP00000490508.1:p.Gly107ProfsTer21
ENST00000636471.1:c.650_653dup	ENSP00000490317.1:p.Gly219ProfsTer21
ENST00000636732.2:c.*367_*370dup	ENSP00000490175.1:n.*367_*370dup
ENST00000636820.1:n.750_753dup
ENST00000637045.1:c.314_317dup	ENSP00000490141.1:p.Gly107ProfsTer21
ENST00000637267.2:c.650_653dup	ENSP00000490293.2:p.Gly219ProfsTer21
ENST00000637304.1:c.314_317dup	ENSP00000490872.1:p.Gly107ProfsTer21
ENST00000638007.1:c.314_317dup	ENSP00000490723.1:p.Gly107ProfsTer21
ENST00000638087.1:c.314_317dup	ENSP00000490673.1:p.Gly107ProfsTer21
ENST00000638128.1:c.-128_-125dup	ENSP00000490934.1:n.-128_-125dup
ENST00000675069.1:c.-133-5223_-133-5220dup	ENSP00000502467.1:n.-133-5223_-133-5220du...
ENST00000303660.8:c.647_650dup	ENSP00000302501.4:p.Gly218ProfsTer21
ENST00000392861.6:c.734_737dup	ENSP00000376601.3:p.Gly247ProfsTer21
ENST00000409487.7:c.650_653dup	ENSP00000386854.2:p.Gly219ProfsTer21
ENST00000419938.5:c.389_392dup	ENSP00000394777.2:p.Gly132ProfsTer21
ENST00000427902.5:c.737_740dup	ENSP00000395496.2:p.Gly248ProfsTer21
ENST00000440875.5:c.635_638dup	ENSP00000475553.2:p.Gly214ProfsTer21
ENST00000497268.1:n.596_599dup
ENST00000539609.7:c.578_581dup	ENSP00000443792.2:p.Gly195ProfsTer21
ENST00000558170.6:c.650_653dup	ENSP00000454157.1:p.Gly219ProfsTer21
ENST00000627532.2:c.650_653dup	ENSP00000487174.1:p.Gly219ProfsTer21
NM_001171653.1:c.578_581dup	NP_001165124.1:p.Gly195ProfsTer21
NM_014795.3:c.650_653dup	NP_055610.1:p.Gly219ProfsTer21
XM_006712881.2:c.650_653dup	XP_006712944.1:p.Gly219ProfsTer21
XM_006712882.2:c.650_653dup	XP_006712945.1:p.Gly219ProfsTer21
XM_011512231.1:c.641_644dup	XP_011510533.1:p.Gly216ProfsTer21
XM_011512232.1:c.629_632dup	XP_011510534.1:p.Gly212ProfsTer21
NM_014795.4:c.650_653dup MANE Select	NP_055610.1:p.Gly219ProfsTer21
NM_001171653.2:c.578_581dup	NP_001165124.1:p.Gly195ProfsTer21