Canonical Allele Identifier: CA429445969

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145157337delT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399770del , CM000664.2:g.144399770del	GRCh38
NC_000002.11:g.145157337del , CM000664.1:g.145157337del	GRCh37
NC_000002.10:g.144873807del	NCBI36
NG_016431.1:g.125622del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1266del	ENSP00000508434.1:n.*1266del
ENST00000440875.6:c.640del	ENSP00000475553.3:p.Arg214GlyfsTer14
ENST00000627532.3:c.1417del MANE Select	ENSP00000487174.1:p.Arg473GlyfsTer14
ENST00000636026.2:c.1417del	ENSP00000490776.1:p.Arg473GlyfsTer14
ENST00000636179.1:n.1386del
ENST00000636413.1:c.1081del	ENSP00000490508.1:p.Arg361GlyfsTer14
ENST00000636471.1:c.1492del	ENSP00000490317.1:p.Arg498GlyfsTer14
ENST00000636732.2:c.*1134del	ENSP00000490175.1:n.*1134del
ENST00000636820.1:n.1517del
ENST00000637045.1:c.1081del	ENSP00000490141.1:p.Arg361GlyfsTer14
ENST00000637267.2:c.1417del	ENSP00000490293.2:p.Arg473GlyfsTer14
ENST00000637304.1:c.1081del	ENSP00000490872.1:p.Arg361GlyfsTer14
ENST00000638007.1:c.1081del	ENSP00000490723.1:p.Arg361GlyfsTer14
ENST00000638087.1:c.1081del	ENSP00000490673.1:p.Arg361GlyfsTer14
ENST00000638128.1:c.640del	ENSP00000490934.1:p.Arg214GlyfsTer14
ENST00000675069.1:c.-133-920del	ENSP00000502467.1:n.-133-920del
ENST00000675145.1:n.1965del
ENST00000303660.8:c.1414del	ENSP00000302501.4:p.Arg472GlyfsTer14
ENST00000409487.7:c.1417del	ENSP00000386854.2:p.Arg473GlyfsTer14
ENST00000419938.5:c.655+1429del	ENSP00000394777.2:n.655+1429del
ENST00000427902.5:c.1504del	ENSP00000395496.2:p.Arg502GlyfsTer14
ENST00000440875.5:c.1154-220del	ENSP00000475553.2:n.1154-220del
ENST00000539609.7:c.1345del	ENSP00000443792.2:p.Arg449GlyfsTer14
ENST00000558170.6:c.1417del	ENSP00000454157.1:p.Arg473GlyfsTer14
ENST00000627532.2:c.1417del	ENSP00000487174.1:p.Arg473GlyfsTer14
NM_001171653.1:c.1345del	NP_001165124.1:p.Arg449GlyfsTer14
NM_014795.3:c.1417del	NP_055610.1:p.Arg473GlyfsTer14
XM_006712881.2:c.1417del	XP_006712944.1:p.Arg473GlyfsTer14
XM_006712882.2:c.1417del	XP_006712945.1:p.Arg473GlyfsTer14
XM_011512231.1:c.1408del	XP_011510533.1:p.Arg470GlyfsTer14
XM_011512232.1:c.1396del	XP_011510534.1:p.Arg466GlyfsTer14
NM_014795.4:c.1417del MANE Select	NP_055610.1:p.Arg473GlyfsTer14
NM_001171653.2:c.1345del	NP_001165124.1:p.Arg449GlyfsTer14