Canonical Allele Identifier: CA429446011

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145157404A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399837A>G , CM000664.2:g.144399837A>G	GRCh38
NC_000002.11:g.145157404A>G , CM000664.1:g.145157404A>G	GRCh37
NC_000002.10:g.144873874A>G	NCBI36
NG_016431.1:g.125555T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1199T>C	ENSP00000508434.1:n.*1199T>C
ENST00000440875.6:c.573T>C	ENSP00000475553.3:p.Phe191=
ENST00000627532.3:c.1350T>C MANE Select	ENSP00000487174.1:p.Phe450=
ENST00000636026.2:c.1350T>C	ENSP00000490776.1:p.Phe450=
ENST00000636179.1:n.1319T>C
ENST00000636413.1:c.1014T>C	ENSP00000490508.1:p.Phe338=
ENST00000636471.1:c.1425T>C	ENSP00000490317.1:p.Phe475=
ENST00000636732.2:c.*1067T>C	ENSP00000490175.1:n.*1067T>C
ENST00000636820.1:n.1450T>C
ENST00000637045.1:c.1014T>C	ENSP00000490141.1:p.Phe338=
ENST00000637267.2:c.1350T>C	ENSP00000490293.2:p.Phe450=
ENST00000637304.1:c.1014T>C	ENSP00000490872.1:p.Phe338=
ENST00000638007.1:c.1014T>C	ENSP00000490723.1:p.Phe338=
ENST00000638087.1:c.1014T>C	ENSP00000490673.1:p.Phe338=
ENST00000638128.1:c.573T>C	ENSP00000490934.1:p.Phe191=
ENST00000675069.1:c.-133-987T>C	ENSP00000502467.1:n.-133-987T>C
ENST00000675145.1:n.1898T>C
ENST00000303660.8:c.1347T>C	ENSP00000302501.4:p.Phe449=
ENST00000409487.7:c.1350T>C	ENSP00000386854.2:p.Phe450=
ENST00000419938.5:c.655+1362T>C	ENSP00000394777.2:n.655+1362T>C
ENST00000427902.5:c.1437T>C	ENSP00000395496.2:p.Phe479=
ENST00000440875.5:c.1153+182T>C	ENSP00000475553.2:n.1153+182T>C
ENST00000539609.7:c.1278T>C	ENSP00000443792.2:p.Phe426=
ENST00000558170.6:c.1350T>C	ENSP00000454157.1:p.Phe450=
ENST00000627532.2:c.1350T>C	ENSP00000487174.1:p.Phe450=
NM_001171653.1:c.1278T>C	NP_001165124.1:p.Phe426=
NM_014795.3:c.1350T>C	NP_055610.1:p.Phe450=
XM_006712881.2:c.1350T>C	XP_006712944.1:p.Phe450=
XM_006712882.2:c.1350T>C	XP_006712945.1:p.Phe450=
XM_011512231.1:c.1341T>C	XP_011510533.1:p.Phe447=
XM_011512232.1:c.1329T>C	XP_011510534.1:p.Phe443=
NM_014795.4:c.1350T>C MANE Select	NP_055610.1:p.Phe450=
NM_001171653.2:c.1278T>C	NP_001165124.1:p.Phe426=