Canonical Allele Identifier: CA658766349

Gene: ZEB2

Linked Data

• PubMed: PMID:26785492

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389625del , CM000664.2:g.144389625del	GRCh38
NC_000002.11:g.145147192del , CM000664.1:g.145147192del	GRCh37
NC_000002.10:g.144863662del	NCBI36
NG_016431.1:g.135767del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3320del	ENSP00000508434.1:n.*3320del
ENST00000440875.6:c.2694del	ENSP00000475553.3:p.Asp898GlufsTer?
ENST00000627532.3:c.3471del MANE Select	ENSP00000487174.1:p.Asp1157GlufsTer?
ENST00000636026.2:c.3359del	ENSP00000490776.1:p.Thr1120ArgfsTer11
ENST00000636179.1:n.3440del
ENST00000636413.1:c.3135del	ENSP00000490508.1:p.Asp1045GlufsTer?
ENST00000636471.1:c.3546del	ENSP00000490317.1:p.Asp1182GlufsTer?
ENST00000636732.2:c.*3188del	ENSP00000490175.1:n.*3188del
ENST00000636820.1:n.3571del
ENST00000637045.1:c.3135del	ENSP00000490141.1:p.Asp1045GlufsTer?
ENST00000637304.1:c.3135del	ENSP00000490872.1:p.Asp1045GlufsTer?
ENST00000638007.1:c.3135del	ENSP00000490723.1:p.Asp1045GlufsTer?
ENST00000638087.1:c.3135del	ENSP00000490673.1:p.Asp1045GlufsTer?
ENST00000638128.1:c.2694del	ENSP00000490934.1:p.Asp898GlufsTer?
ENST00000639389.1:c.151+6787del	ENSP00000492572.1:n.151+6787del
ENST00000647488.1:c.691del	ENSP00000494820.1:n.691del
ENST00000675069.1:c.1002del	ENSP00000502467.1:p.Asp334GlufsTer?
ENST00000303660.8:c.3468del	ENSP00000302501.4:p.Asp1156GlufsTer?
ENST00000409487.7:c.3471del	ENSP00000386854.2:p.Asp1157GlufsTer?
ENST00000419938.5:c.656-743del	ENSP00000394777.2:n.656-743del
ENST00000539609.7:c.3399del	ENSP00000443792.2:p.Asp1133GlufsTer?
ENST00000558170.6:c.3471del	ENSP00000454157.1:p.Asp1157GlufsTer?
ENST00000627532.2:c.3471del	ENSP00000487174.1:p.Asp1157GlufsTer?
NM_001171653.1:c.3399del	NP_001165124.1:p.Asp1133GlufsTer?
NM_014795.3:c.3471del	NP_055610.1:p.Asp1157GlufsTer?
XM_006712881.2:c.3471del	XP_006712944.1:p.Asp1157GlufsTer?
XM_006712882.2:c.3471del	XP_006712945.1:p.Asp1157GlufsTer?
XM_011512231.1:c.3462del	XP_011510533.1:p.Asp1154GlufsTer?
XM_011512232.1:c.3450del	XP_011510534.1:p.Asp1150GlufsTer?
NM_014795.4:c.3471del MANE Select	NP_055610.1:p.Asp1157GlufsTer?
NM_001171653.2:c.3399del	NP_001165124.1:p.Asp1133GlufsTer?