Canonical Allele Identifier: CA1294885354

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399638_144399646delinsTCACTACCG , CM000664.2:g.144399638_144399646delinsTCACTACCG	GRCh38
NC_000002.11:g.145157205_145157213delinsTCACTACCG , CM000664.1:g.145157205_145157213delinsTCACTACCG	GRCh37
NC_000002.10:g.144873675_144873683delinsTCACTACCG	NCBI36
NG_016431.1:g.125746_125754delinsCGGTAGTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1390_*1398delinsCGGTAGTGA	ENSP00000508434.1:n.*1390_*1398delinsCGGTAGTGA
ENST00000440875.6:c.764_772delinsCGGTAGTGA	ENSP00000475553.3:p.Pro255=
ENST00000627532.3:c.1541_1549delinsCGGTAGTGA MANE Select	ENSP00000487174.1:p.Pro514=
ENST00000636026.2:c.1541_1549delinsCGGTAGTGA	ENSP00000490776.1:p.Pro514=
ENST00000636179.1:n.1510_1518delinsCGGTAGTGA
ENST00000636413.1:c.1205_1213delinsCGGTAGTGA	ENSP00000490508.1:p.Pro402=
ENST00000636471.1:c.1616_1624delinsCGGTAGTGA	ENSP00000490317.1:p.Pro539=
ENST00000636732.2:c.*1258_*1266delinsCGGTAGTGA	ENSP00000490175.1:n.*1258_*1266delinsCGGTAGTGA
ENST00000636820.1:n.1641_1649delinsCGGTAGTGA
ENST00000637045.1:c.1205_1213delinsCGGTAGTGA	ENSP00000490141.1:p.Pro402=
ENST00000637267.2:c.1541_1549delinsCGGTAGTGA	ENSP00000490293.2:p.Pro514=
ENST00000637304.1:c.1205_1213delinsCGGTAGTGA	ENSP00000490872.1:p.Pro402=
ENST00000638007.1:c.1205_1213delinsCGGTAGTGA	ENSP00000490723.1:p.Pro402=
ENST00000638087.1:c.1205_1213delinsCGGTAGTGA	ENSP00000490673.1:p.Pro402=
ENST00000638128.1:c.764_772delinsCGGTAGTGA	ENSP00000490934.1:p.Pro255=
ENST00000675069.1:c.-133-796_-133-788delinsCGGTAGTGA	ENSP00000502467.1:n.-133-796_-133-788delinsCGGTAGTGA
ENST00000675145.1:n.2089_2097delinsCGGTAGTGA
ENST00000303660.8:c.1538_1546delinsCGGTAGTGA	ENSP00000302501.4:p.Pro513=
ENST00000409487.7:c.1541_1549delinsCGGTAGTGA	ENSP00000386854.2:p.Pro514=
ENST00000419938.5:c.655+1553_655+1561delinsCGGTAGTGA	ENSP00000394777.2:n.655+1553_655+1561delinsCGGTAGTGA
ENST00000427902.5:c.1628_1636delinsCGGTAGTGA	ENSP00000395496.2:p.Pro543=
ENST00000440875.5:c.1154-96_1154-88delinsCGGTAGTGA	ENSP00000475553.2:n.1154-96_1154-88delinsCGGTAGTGA
ENST00000539609.7:c.1469_1477delinsCGGTAGTGA	ENSP00000443792.2:p.Pro490=
ENST00000558170.6:c.1541_1549delinsCGGTAGTGA	ENSP00000454157.1:p.Pro514=
ENST00000627532.2:c.1541_1549delinsCGGTAGTGA	ENSP00000487174.1:p.Pro514=
NM_001171653.1:c.1469_1477delinsCGGTAGTGA	NP_001165124.1:p.Pro490=
NM_014795.3:c.1541_1549delinsCGGTAGTGA	NP_055610.1:p.Pro514=
XM_006712881.2:c.1541_1549delinsCGGTAGTGA	XP_006712944.1:p.Pro514=
XM_006712882.2:c.1541_1549delinsCGGTAGTGA	XP_006712945.1:p.Pro514=
XM_011512231.1:c.1532_1540delinsCGGTAGTGA	XP_011510533.1:p.Pro511=
XM_011512232.1:c.1520_1528delinsCGGTAGTGA	XP_011510534.1:p.Pro507=
NM_014795.4:c.1541_1549delinsCGGTAGTGA MANE Select	NP_055610.1:p.Pro514=
NM_001171653.2:c.1469_1477delinsCGGTAGTGA	NP_001165124.1:p.Pro490=