Canonical Allele Identifier: CA429445659

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156960C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399393C>T , CM000664.2:g.144399393C>T	GRCh38
NC_000002.11:g.145156960C>T , CM000664.1:g.145156960C>T	GRCh37
NC_000002.10:g.144873430C>T	NCBI36
NG_016431.1:g.125999G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1643G>A	ENSP00000508434.1:n.*1643G>A
ENST00000440875.6:c.1017G>A	ENSP00000475553.3:p.Gln339=
ENST00000627532.3:c.1794G>A MANE Select	ENSP00000487174.1:p.Gln598=
ENST00000636026.2:c.1794G>A	ENSP00000490776.1:p.Gln598=
ENST00000636179.1:n.1763G>A
ENST00000636413.1:c.1458G>A	ENSP00000490508.1:p.Gln486=
ENST00000636471.1:c.1869G>A	ENSP00000490317.1:p.Gln623=
ENST00000636732.2:c.*1511G>A	ENSP00000490175.1:n.*1511G>A
ENST00000636820.1:n.1894G>A
ENST00000637045.1:c.1458G>A	ENSP00000490141.1:p.Gln486=
ENST00000637267.2:c.1794G>A	ENSP00000490293.2:p.Gln598=
ENST00000637304.1:c.1458G>A	ENSP00000490872.1:p.Gln486=
ENST00000638007.1:c.1458G>A	ENSP00000490723.1:p.Gln486=
ENST00000638087.1:c.1458G>A	ENSP00000490673.1:p.Gln486=
ENST00000638128.1:c.1017G>A	ENSP00000490934.1:p.Gln339=
ENST00000675069.1:c.-133-543G>A	ENSP00000502467.1:n.-133-543G>A
ENST00000675145.1:n.2342G>A
ENST00000303660.8:c.1791G>A	ENSP00000302501.4:p.Gln597=
ENST00000409487.7:c.1794G>A	ENSP00000386854.2:p.Gln598=
ENST00000419938.5:c.655+1806G>A	ENSP00000394777.2:n.655+1806G>A
ENST00000427902.5:c.1881G>A	ENSP00000395496.2:p.Gln627=
ENST00000440875.5:c.1167+144G>A	ENSP00000475553.2:n.1167+144G>A
ENST00000539609.7:c.1722G>A	ENSP00000443792.2:p.Gln574=
ENST00000558170.6:c.1794G>A	ENSP00000454157.1:p.Gln598=
ENST00000627532.2:c.1794G>A	ENSP00000487174.1:p.Gln598=
NM_001171653.1:c.1722G>A	NP_001165124.1:p.Gln574=
NM_014795.3:c.1794G>A	NP_055610.1:p.Gln598=
XM_006712881.2:c.1794G>A	XP_006712944.1:p.Gln598=
XM_006712882.2:c.1794G>A	XP_006712945.1:p.Gln598=
XM_011512231.1:c.1785G>A	XP_011510533.1:p.Gln595=
XM_011512232.1:c.1773G>A	XP_011510534.1:p.Gln591=
NM_014795.4:c.1794G>A MANE Select	NP_055610.1:p.Gln598=
NM_001171653.2:c.1722G>A	NP_001165124.1:p.Gln574=