Canonical Allele Identifier: CA1294885407

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399763T= , CM000664.2:g.144399763T=	GRCh38
NC_000002.11:g.145157330T= , CM000664.1:g.145157330T=	GRCh37
NC_000002.10:g.144873800T=	NCBI36
NG_016431.1:g.125629A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1273A=	ENSP00000508434.1:n.*1273A=
ENST00000440875.6:c.647A=	ENSP00000475553.3:p.Lys216=
ENST00000627532.3:c.1424A= MANE Select	ENSP00000487174.1:p.Lys475=
ENST00000636026.2:c.1424A=	ENSP00000490776.1:p.Lys475=
ENST00000636179.1:n.1393A=
ENST00000636413.1:c.1088A=	ENSP00000490508.1:p.Lys363=
ENST00000636471.1:c.1499A=	ENSP00000490317.1:p.Lys500=
ENST00000636732.2:c.*1141A=	ENSP00000490175.1:n.*1141A=
ENST00000636820.1:n.1524A=
ENST00000637045.1:c.1088A=	ENSP00000490141.1:p.Lys363=
ENST00000637267.2:c.1424A=	ENSP00000490293.2:p.Lys475=
ENST00000637304.1:c.1088A=	ENSP00000490872.1:p.Lys363=
ENST00000638007.1:c.1088A=	ENSP00000490723.1:p.Lys363=
ENST00000638087.1:c.1088A=	ENSP00000490673.1:p.Lys363=
ENST00000638128.1:c.647A=	ENSP00000490934.1:p.Lys216=
ENST00000675069.1:c.-133-913A=	ENSP00000502467.1:n.-133-913A=
ENST00000675145.1:n.1972A=
ENST00000303660.8:c.1421A=	ENSP00000302501.4:p.Lys474=
ENST00000409487.7:c.1424A=	ENSP00000386854.2:p.Lys475=
ENST00000419938.5:c.655+1436A=	ENSP00000394777.2:n.655+1436A=
ENST00000427902.5:c.1511A=	ENSP00000395496.2:p.Lys504=
ENST00000440875.5:c.1154-213A=	ENSP00000475553.2:n.1154-213A=
ENST00000539609.7:c.1352A=	ENSP00000443792.2:p.Lys451=
ENST00000558170.6:c.1424A=	ENSP00000454157.1:p.Lys475=
ENST00000627532.2:c.1424A=	ENSP00000487174.1:p.Lys475=
NM_001171653.1:c.1352A=	NP_001165124.1:p.Lys451=
NM_014795.3:c.1424A=	NP_055610.1:p.Lys475=
XM_006712881.2:c.1424A=	XP_006712944.1:p.Lys475=
XM_006712882.2:c.1424A=	XP_006712945.1:p.Lys475=
XM_011512231.1:c.1415A=	XP_011510533.1:p.Lys472=
XM_011512232.1:c.1403A=	XP_011510534.1:p.Lys468=
NM_014795.4:c.1424A= MANE Select	NP_055610.1:p.Lys475=
NM_001171653.2:c.1352A=	NP_001165124.1:p.Lys451=