Canonical Allele Identifier: CA276969

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 212634
• ClinVar RCV Id: RCV000192418
• dbSNP Id: rs797046119
• MyVariant Identifiers: chr2:g.145156347_145156350del (hg19) ; chr2:g.144398780_144398783del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398781_144398784del , CM000664.2:g.144398781_144398784del	GRCh38
NC_000002.11:g.145156348_145156351del , CM000664.1:g.145156348_145156351del	GRCh37
NC_000002.10:g.144872818_144872821del	NCBI36
NG_016431.1:g.126609_126612del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2253_*2256del	ENSP00000508434.1:n.*2253_*2256del
ENST00000440875.6:c.1627_1630del	ENSP00000475553.3:p.Thr543GlnfsTer14
ENST00000627532.3:c.2404_2407del MANE Select	ENSP00000487174.1:p.Thr802GlnfsTer14
ENST00000636026.2:c.2404_2407del	ENSP00000490776.1:p.Thr802GlnfsTer14
ENST00000636179.1:n.2373_2376del
ENST00000636413.1:c.2068_2071del	ENSP00000490508.1:p.Thr690GlnfsTer14
ENST00000636471.1:c.2479_2482del	ENSP00000490317.1:p.Thr827GlnfsTer14
ENST00000636732.2:c.*2121_*2124del	ENSP00000490175.1:n.*2121_*2124del
ENST00000636820.1:n.2504_2507del
ENST00000637045.1:c.2068_2071del	ENSP00000490141.1:p.Thr690GlnfsTer14
ENST00000637304.1:c.2068_2071del	ENSP00000490872.1:p.Thr690GlnfsTer14
ENST00000638007.1:c.2068_2071del	ENSP00000490723.1:p.Thr690GlnfsTer14
ENST00000638087.1:c.2068_2071del	ENSP00000490673.1:p.Thr690GlnfsTer14
ENST00000638128.1:c.1627_1630del	ENSP00000490934.1:p.Thr543GlnfsTer14
ENST00000675069.1:c.-66_-63del	ENSP00000502467.1:n.-66_-63del
ENST00000675145.1:n.2952_2955del
ENST00000303660.8:c.2401_2404del	ENSP00000302501.4:p.Thr801GlnfsTer14
ENST00000409487.7:c.2404_2407del	ENSP00000386854.2:p.Thr802GlnfsTer14
ENST00000419938.5:c.655+2416_655+2419del	ENSP00000394777.2:n.655+2416_655+2419del
ENST00000440875.5:c.1167+754_1167+757del	ENSP00000475553.2:n.1167+754_1167+757del
ENST00000539609.7:c.2332_2335del	ENSP00000443792.2:p.Thr778GlnfsTer14
ENST00000558170.6:c.2404_2407del	ENSP00000454157.1:p.Thr802GlnfsTer14
ENST00000627532.2:c.2404_2407del	ENSP00000487174.1:p.Thr802GlnfsTer14
NM_001171653.1:c.2332_2335del	NP_001165124.1:p.Thr778GlnfsTer14
NM_014795.3:c.2404_2407del	NP_055610.1:p.Thr802GlnfsTer14
XM_006712881.2:c.2404_2407del	XP_006712944.1:p.Thr802GlnfsTer14
XM_006712882.2:c.2404_2407del	XP_006712945.1:p.Thr802GlnfsTer14
XM_011512231.1:c.2395_2398del	XP_011510533.1:p.Thr799GlnfsTer14
XM_011512232.1:c.2383_2386del	XP_011510534.1:p.Thr795GlnfsTer14
NM_014795.4:c.2404_2407del MANE Select	NP_055610.1:p.Thr802GlnfsTer14
NM_001171653.2:c.2332_2335del	NP_001165124.1:p.Thr778GlnfsTer14