Canonical Allele Identifier: CA348708395

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156363G>T (hg19) ; chr2:g.144398796G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398796G>T , CM000664.2:g.144398796G>T	GRCh38
NC_000002.11:g.145156363G>T , CM000664.1:g.145156363G>T	GRCh37
NC_000002.10:g.144872833G>T	NCBI36
NG_016431.1:g.126596C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2240C>A	ENSP00000508434.1:n.*2240C>A
ENST00000440875.6:c.1614C>A	ENSP00000475553.3:p.His538Gln
ENST00000627532.3:c.2391C>A MANE Select	ENSP00000487174.1:p.His797Gln
ENST00000636026.2:c.2391C>A	ENSP00000490776.1:p.His797Gln
ENST00000636179.1:n.2360C>A
ENST00000636413.1:c.2055C>A	ENSP00000490508.1:p.His685Gln
ENST00000636471.1:c.2466C>A	ENSP00000490317.1:p.His822Gln
ENST00000636732.2:c.*2108C>A	ENSP00000490175.1:n.*2108C>A
ENST00000636820.1:n.2491C>A
ENST00000637045.1:c.2055C>A	ENSP00000490141.1:p.His685Gln
ENST00000637304.1:c.2055C>A	ENSP00000490872.1:p.His685Gln
ENST00000638007.1:c.2055C>A	ENSP00000490723.1:p.His685Gln
ENST00000638087.1:c.2055C>A	ENSP00000490673.1:p.His685Gln
ENST00000638128.1:c.1614C>A	ENSP00000490934.1:p.His538Gln
ENST00000675069.1:c.-79C>A	ENSP00000502467.1:n.-79C>A
ENST00000675145.1:n.2939C>A
ENST00000303660.8:c.2388C>A	ENSP00000302501.4:p.His796Gln
ENST00000409487.7:c.2391C>A	ENSP00000386854.2:p.His797Gln
ENST00000419938.5:c.655+2403C>A	ENSP00000394777.2:n.655+2403C>A
ENST00000440875.5:c.1167+741C>A	ENSP00000475553.2:n.1167+741C>A
ENST00000539609.7:c.2319C>A	ENSP00000443792.2:p.His773Gln
ENST00000558170.6:c.2391C>A	ENSP00000454157.1:p.His797Gln
ENST00000627532.2:c.2391C>A	ENSP00000487174.1:p.His797Gln
NM_001171653.1:c.2319C>A	NP_001165124.1:p.His773Gln
NM_014795.3:c.2391C>A	NP_055610.1:p.His797Gln
XM_006712881.2:c.2391C>A	XP_006712944.1:p.His797Gln
XM_006712882.2:c.2391C>A	XP_006712945.1:p.His797Gln
XM_011512231.1:c.2382C>A	XP_011510533.1:p.His794Gln
XM_011512232.1:c.2370C>A	XP_011510534.1:p.His790Gln
NM_014795.4:c.2391C>A MANE Select	NP_055610.1:p.His797Gln
NM_001171653.2:c.2319C>A	NP_001165124.1:p.His773Gln