Canonical Allele Identifier: CA274511

Gene: ZEB2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399645_144399646insT , CM000664.2:g.144399645_144399646insT	GRCh38
NC_000002.11:g.145157212_145157213insT , CM000664.1:g.145157212_145157213insT	GRCh37
NC_000002.10:g.144873682_144873683insT	NCBI36
NG_016431.1:g.125746_125747insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1390_*1391insA	ENSP00000508434.1:n.*1390_*1391insA
ENST00000440875.6:c.764_765insA	ENSP00000475553.3:p.Val256GlyfsTer5
ENST00000627532.3:c.1541_1542insA MANE Select	ENSP00000487174.1:p.Val515GlyfsTer5
ENST00000636026.2:c.1541_1542insA	ENSP00000490776.1:p.Val515GlyfsTer5
ENST00000636179.1:n.1510_1511insA
ENST00000636413.1:c.1205_1206insA	ENSP00000490508.1:p.Val403GlyfsTer5
ENST00000636471.1:c.1616_1617insA	ENSP00000490317.1:p.Val540GlyfsTer5
ENST00000636732.2:c.*1258_*1259insA	ENSP00000490175.1:n.*1258_*1259insA
ENST00000636820.1:n.1641_1642insA
ENST00000637045.1:c.1205_1206insA	ENSP00000490141.1:p.Val403GlyfsTer5
ENST00000637267.2:c.1541_1542insA	ENSP00000490293.2:p.Val515GlyfsTer5
ENST00000637304.1:c.1205_1206insA	ENSP00000490872.1:p.Val403GlyfsTer5
ENST00000638007.1:c.1205_1206insA	ENSP00000490723.1:p.Val403GlyfsTer5
ENST00000638087.1:c.1205_1206insA	ENSP00000490673.1:p.Val403GlyfsTer5
ENST00000638128.1:c.764_765insA	ENSP00000490934.1:p.Val256GlyfsTer5
ENST00000675069.1:c.-133-796_-133-795insA	ENSP00000502467.1:n.-133-796_-133-795insA
ENST00000675145.1:n.2089_2090insA
ENST00000303660.8:c.1538_1539insA	ENSP00000302501.4:p.Val514GlyfsTer5
ENST00000409487.7:c.1541_1542insA	ENSP00000386854.2:p.Val515GlyfsTer5
ENST00000419938.5:c.655+1553_655+1554insA	ENSP00000394777.2:n.655+1553_655+1554insA
ENST00000427902.5:c.1628_1629insA	ENSP00000395496.2:p.Val544GlyfsTer5
ENST00000440875.5:c.1154-96_1154-95insA	ENSP00000475553.2:n.1154-96_1154-95insA
ENST00000539609.7:c.1469_1470insA	ENSP00000443792.2:p.Val491GlyfsTer5
ENST00000558170.6:c.1541_1542insA	ENSP00000454157.1:p.Val515GlyfsTer5
ENST00000627532.2:c.1541_1542insA	ENSP00000487174.1:p.Val515GlyfsTer5
NM_001171653.1:c.1469_1470insA	NP_001165124.1:p.Val491GlyfsTer5
NM_014795.3:c.1541_1542insA	NP_055610.1:p.Val515GlyfsTer5
XM_006712881.2:c.1541_1542insA	XP_006712944.1:p.Val515GlyfsTer5
XM_006712882.2:c.1541_1542insA	XP_006712945.1:p.Val515GlyfsTer5
XM_011512231.1:c.1532_1533insA	XP_011510533.1:p.Val512GlyfsTer5
XM_011512232.1:c.1520_1521insA	XP_011510534.1:p.Val508GlyfsTer5
NM_014795.4:c.1541_1542insA MANE Select	NP_055610.1:p.Val515GlyfsTer5
NM_001171653.2:c.1469_1470insA	NP_001165124.1:p.Val491GlyfsTer5