Canonical Allele Identifier: CA2586963957

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 2627885
• ClinVar RCV Id: RCV003389229

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399804_144399805del , CM000664.2:g.144399804_144399805del	GRCh38
NC_000002.11:g.145157371_145157372del , CM000664.1:g.145157371_145157372del	GRCh37
NC_000002.10:g.144873841_144873842del	NCBI36
NG_016431.1:g.125589_125590del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1233_*1234del	ENSP00000508434.1:n.*1233_*1234del
ENST00000440875.6:c.607_608del	ENSP00000475553.3:p.Lys203GlyfsTer19
ENST00000627532.3:c.1384_1385del MANE Select	ENSP00000487174.1:p.Lys462GlyfsTer19
ENST00000636026.2:c.1384_1385del	ENSP00000490776.1:p.Lys462GlyfsTer19
ENST00000636179.1:n.1353_1354del
ENST00000636413.1:c.1048_1049del	ENSP00000490508.1:p.Lys350GlyfsTer19
ENST00000636471.1:c.1459_1460del	ENSP00000490317.1:p.Lys487GlyfsTer19
ENST00000636732.2:c.*1101_*1102del	ENSP00000490175.1:n.*1101_*1102del
ENST00000636820.1:n.1484_1485del
ENST00000637045.1:c.1048_1049del	ENSP00000490141.1:p.Lys350GlyfsTer19
ENST00000637267.2:c.1384_1385del	ENSP00000490293.2:p.Lys462GlyfsTer19
ENST00000637304.1:c.1048_1049del	ENSP00000490872.1:p.Lys350GlyfsTer19
ENST00000638007.1:c.1048_1049del	ENSP00000490723.1:p.Lys350GlyfsTer19
ENST00000638087.1:c.1048_1049del	ENSP00000490673.1:p.Lys350GlyfsTer19
ENST00000638128.1:c.607_608del	ENSP00000490934.1:p.Lys203GlyfsTer19
ENST00000675069.1:c.-133-953_-133-952del	ENSP00000502467.1:n.-133-953_-133-952del
ENST00000675145.1:n.1932_1933del
ENST00000303660.8:c.1381_1382del	ENSP00000302501.4:p.Lys461GlyfsTer19
ENST00000409487.7:c.1384_1385del	ENSP00000386854.2:p.Lys462GlyfsTer19
ENST00000419938.5:c.655+1396_655+1397del	ENSP00000394777.2:n.655+1396_655+1397del
ENST00000427902.5:c.1471_1472del	ENSP00000395496.2:p.Lys491GlyfsTer19
ENST00000440875.5:c.1153+216_1153+217del	ENSP00000475553.2:n.1153+216_1153+217del
ENST00000539609.7:c.1312_1313del	ENSP00000443792.2:p.Lys438GlyfsTer19
ENST00000558170.6:c.1384_1385del	ENSP00000454157.1:p.Lys462GlyfsTer19
ENST00000627532.2:c.1384_1385del	ENSP00000487174.1:p.Lys462GlyfsTer19
NM_001171653.1:c.1312_1313del	NP_001165124.1:p.Lys438GlyfsTer19
NM_014795.3:c.1384_1385del	NP_055610.1:p.Lys462GlyfsTer19
XM_006712881.2:c.1384_1385del	XP_006712944.1:p.Lys462GlyfsTer19
XM_006712882.2:c.1384_1385del	XP_006712945.1:p.Lys462GlyfsTer19
XM_011512231.1:c.1375_1376del	XP_011510533.1:p.Lys459GlyfsTer19
XM_011512232.1:c.1363_1364del	XP_011510534.1:p.Lys455GlyfsTer19
NM_014795.4:c.1384_1385del MANE Select	NP_055610.1:p.Lys462GlyfsTer19
NM_001171653.2:c.1312_1313del	NP_001165124.1:p.Lys438GlyfsTer19