Canonical Allele Identifier: CA916670961

Gene: ZEB2

Linked Data

• dbSNP Id: rs1573716641

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399405_144399406insGA , CM000664.2:g.144399405_144399406insGA	GRCh38
NC_000002.11:g.145156972_145156973insGA , CM000664.1:g.145156972_145156973insGA	GRCh37
NC_000002.10:g.144873442_144873443insGA	NCBI36
NG_016431.1:g.125986_125987insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1630_*1631insTC	ENSP00000508434.1:n.*1630_*1631insTC
ENST00000440875.6:c.1004_1005insTC	ENSP00000475553.3:p.His338CysfsTer11
ENST00000627532.3:c.1781_1782insTC MANE Select	ENSP00000487174.1:p.His597CysfsTer11
ENST00000636026.2:c.1781_1782insTC	ENSP00000490776.1:p.His597CysfsTer11
ENST00000636179.1:n.1750_1751insTC
ENST00000636413.1:c.1445_1446insTC	ENSP00000490508.1:p.His485CysfsTer11
ENST00000636471.1:c.1856_1857insTC	ENSP00000490317.1:p.His622CysfsTer11
ENST00000636732.2:c.*1498_*1499insTC	ENSP00000490175.1:n.*1498_*1499insTC
ENST00000636820.1:n.1881_1882insTC
ENST00000637045.1:c.1445_1446insTC	ENSP00000490141.1:p.His485CysfsTer11
ENST00000637267.2:c.1781_1782insTC	ENSP00000490293.2:p.His597CysfsTer11
ENST00000637304.1:c.1445_1446insTC	ENSP00000490872.1:p.His485CysfsTer11
ENST00000638007.1:c.1445_1446insTC	ENSP00000490723.1:p.His485CysfsTer11
ENST00000638087.1:c.1445_1446insTC	ENSP00000490673.1:p.His485CysfsTer11
ENST00000638128.1:c.1004_1005insTC	ENSP00000490934.1:p.His338CysfsTer11
ENST00000675069.1:c.-133-556_-133-555insTC	ENSP00000502467.1:n.-133-556_-133-555insTC
ENST00000675145.1:n.2329_2330insTC
ENST00000303660.8:c.1778_1779insTC	ENSP00000302501.4:p.His596CysfsTer11
ENST00000409487.7:c.1781_1782insTC	ENSP00000386854.2:p.His597CysfsTer11
ENST00000419938.5:c.655+1793_655+1794insTC	ENSP00000394777.2:n.655+1793_655+1794insTC
ENST00000427902.5:c.1868_1869insTC	ENSP00000395496.2:p.His626CysfsTer11
ENST00000440875.5:c.1167+131_1167+132insTC	ENSP00000475553.2:n.1167+131_1167+132insTC
ENST00000539609.7:c.1709_1710insTC	ENSP00000443792.2:p.His573CysfsTer11
ENST00000558170.6:c.1781_1782insTC	ENSP00000454157.1:p.His597CysfsTer11
ENST00000627532.2:c.1781_1782insTC	ENSP00000487174.1:p.His597CysfsTer11
NM_001171653.1:c.1709_1710insTC	NP_001165124.1:p.His573CysfsTer11
NM_014795.3:c.1781_1782insTC	NP_055610.1:p.His597CysfsTer11
XM_006712881.2:c.1781_1782insTC	XP_006712944.1:p.His597CysfsTer11
XM_006712882.2:c.1781_1782insTC	XP_006712945.1:p.His597CysfsTer11
XM_011512231.1:c.1772_1773insTC	XP_011510533.1:p.His594CysfsTer11
XM_011512232.1:c.1760_1761insTC	XP_011510534.1:p.His590CysfsTer11
NM_014795.4:c.1781_1782insTC MANE Select	NP_055610.1:p.His597CysfsTer11
NM_001171653.2:c.1709_1710insTC	NP_001165124.1:p.His573CysfsTer11