Canonical Allele Identifier: CA758227266

Gene: ZEB2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144429458C>A , CM000664.2:g.144429458C>A	GRCh38
NC_000002.11:g.145187025C>A , CM000664.1:g.145187025C>A	GRCh37
NC_000002.10:g.144903495C>A	NCBI36
NG_016431.1:g.95934G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*252+311G>T	ENSP00000508434.1:n.*252+311G>T
ENST00000440875.6:c.-375+311G>T	ENSP00000475553.3:n.-375+311G>T
ENST00000627532.3:c.331+311G>T MANE Select	ENSP00000487174.1:n.331+311G>T
ENST00000636026.2:c.331+311G>T	ENSP00000490776.1:n.331+311G>T
ENST00000636179.1:n.300+311G>T
ENST00000636413.1:c.-6+311G>T	ENSP00000490508.1:n.-6+311G>T
ENST00000636471.1:c.331+311G>T	ENSP00000490317.1:n.331+311G>T
ENST00000636732.2:c.331+311G>T	ENSP00000490175.1:n.331+311G>T
ENST00000636820.1:n.431+311G>T
ENST00000637045.1:c.-6+311G>T	ENSP00000490141.1:n.-6+311G>T
ENST00000637267.2:c.331+311G>T	ENSP00000490293.2:n.331+311G>T
ENST00000637304.1:c.-6+311G>T	ENSP00000490872.1:n.-6+311G>T
ENST00000638007.1:c.-6+311G>T	ENSP00000490723.1:n.-6+311G>T
ENST00000638087.1:c.-6+311G>T	ENSP00000490673.1:n.-6+311G>T
ENST00000638128.1:c.-375+311G>T	ENSP00000490934.1:n.-375+311G>T
ENST00000675069.1:c.-133-30608G>T	ENSP00000502467.1:n.-133-30608G>T
ENST00000303660.8:c.331+311G>T	ENSP00000302501.4:n.331+311G>T
ENST00000392861.6:c.415+311G>T	ENSP00000376601.3:n.415+311G>T
ENST00000409211.5:c.331+311G>T	ENSP00000387256.2:n.331+311G>T
ENST00000409487.7:c.331+311G>T	ENSP00000386854.2:n.331+311G>T
ENST00000419938.5:c.331+311G>T	ENSP00000394777.2:n.331+311G>T
ENST00000427902.5:c.418+311G>T	ENSP00000395496.2:n.418+311G>T
ENST00000431672.4:c.331+311G>T	ENSP00000475267.2:n.331+311G>T
ENST00000434448.5:c.*262+311G>T	ENSP00000487261.1:n.*262+311G>T
ENST00000440875.5:c.316+311G>T	ENSP00000475553.2:n.316+311G>T
ENST00000465308.5:c.331+311G>T	ENSP00000487476.1:n.331+311G>T
ENST00000472146.5:n.892G>T
ENST00000539609.7:c.331+311G>T	ENSP00000443792.2:n.331+311G>T
ENST00000558170.6:c.331+311G>T	ENSP00000454157.1:n.331+311G>T
ENST00000627532.2:c.331+311G>T	ENSP00000487174.1:n.331+311G>T
ENST00000627856.2:n.291+311G>T
NM_001171653.1:c.331+311G>T	NP_001165124.1:n.331+311G>T
NM_014795.3:c.331+311G>T	NP_055610.1:n.331+311G>T
XM_006712881.2:c.331+311G>T	XP_006712944.1:n.331+311G>T
XM_006712882.2:c.331+311G>T	XP_006712945.1:n.331+311G>T
XM_011512231.1:c.322+311G>T	XP_011510533.1:n.322+311G>T
XM_011512232.1:c.310+311G>T	XP_011510534.1:n.310+311G>T
NM_014795.4:c.331+311G>T MANE Select	NP_055610.1:n.331+311G>T
NM_001171653.2:c.331+311G>T	NP_001165124.1:n.331+311G>T