Canonical Allele Identifier: CA915942801

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 807524
• ClinVar RCV Id: RCV000995678
• dbSNP Id: rs1573721065

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403953_144403954del , CM000664.2:g.144403953_144403954del	GRCh38
NC_000002.11:g.145161520_145161521del , CM000664.1:g.145161520_145161521del	GRCh37
NC_000002.10:g.144877990_144877991del	NCBI36
NG_016431.1:g.121439_121440del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*619_*620del	ENSP00000508434.1:n.*619_*620del
ENST00000440875.6:c.-8_-7del	ENSP00000475553.3:n.-8_-7del
ENST00000627532.3:c.770_771del MANE Select	ENSP00000487174.1:p.Glu257AlafsTer22
ENST00000636026.2:c.770_771del	ENSP00000490776.1:p.Glu257AlafsTer22
ENST00000636179.1:n.739_740del
ENST00000636413.1:c.434_435del	ENSP00000490508.1:p.Glu145AlafsTer22
ENST00000636471.1:c.770_771del	ENSP00000490317.1:p.Glu257AlafsTer22
ENST00000636732.2:c.*487_*488del	ENSP00000490175.1:n.*487_*488del
ENST00000636820.1:n.870_871del
ENST00000637045.1:c.434_435del	ENSP00000490141.1:p.Glu145AlafsTer22
ENST00000637267.2:c.770_771del	ENSP00000490293.2:p.Glu257AlafsTer22
ENST00000637304.1:c.434_435del	ENSP00000490872.1:p.Glu145AlafsTer22
ENST00000638007.1:c.434_435del	ENSP00000490723.1:p.Glu145AlafsTer22
ENST00000638087.1:c.434_435del	ENSP00000490673.1:p.Glu145AlafsTer22
ENST00000638128.1:c.-8_-7del	ENSP00000490934.1:n.-8_-7del
ENST00000675069.1:c.-133-5103_-133-5102del	ENSP00000502467.1:n.-133-5103_-133-5102del
ENST00000303660.8:c.767_768del	ENSP00000302501.4:p.Glu256AlafsTer22
ENST00000392861.6:c.854_855del	ENSP00000376601.3:p.Glu285AlafsTer22
ENST00000409487.7:c.770_771del	ENSP00000386854.2:p.Glu257AlafsTer22
ENST00000419938.5:c.509_510del	ENSP00000394777.2:p.Glu170AlafsTer22
ENST00000427902.5:c.857_858del	ENSP00000395496.2:p.Glu286AlafsTer22
ENST00000440875.5:c.755_756del	ENSP00000475553.2:p.Glu252AlafsTer22
ENST00000539609.7:c.698_699del	ENSP00000443792.2:p.Glu233AlafsTer22
ENST00000558170.6:c.770_771del	ENSP00000454157.1:p.Glu257AlafsTer22
ENST00000627532.2:c.770_771del	ENSP00000487174.1:p.Glu257AlafsTer22
NM_001171653.1:c.698_699del	NP_001165124.1:p.Glu233AlafsTer22
NM_014795.3:c.770_771del	NP_055610.1:p.Glu257AlafsTer22
XM_006712881.2:c.770_771del	XP_006712944.1:p.Glu257AlafsTer22
XM_006712882.2:c.770_771del	XP_006712945.1:p.Glu257AlafsTer22
XM_011512231.1:c.761_762del	XP_011510533.1:p.Glu254AlafsTer22
XM_011512232.1:c.749_750del	XP_011510534.1:p.Glu250AlafsTer22
NM_014795.4:c.770_771del MANE Select	NP_055610.1:p.Glu257AlafsTer22
NM_001171653.2:c.698_699del	NP_001165124.1:p.Glu233AlafsTer22