Canonical Allele Identifier: CA1294881378

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389890G= , CM000664.2:g.144389890G=	GRCh38
NC_000002.11:g.145147457G= , CM000664.1:g.145147457G=	GRCh37
NC_000002.10:g.144863927G=	NCBI36
NG_016431.1:g.135502C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3055C=	ENSP00000508434.1:n.*3055C=
ENST00000440875.6:c.2429C=	ENSP00000475553.3:p.Ser810=
ENST00000627532.3:c.3206C= MANE Select	ENSP00000487174.1:p.Ser1069=
ENST00000636026.2:c.3206C=	ENSP00000490776.1:p.Ser1069=
ENST00000636179.1:n.3175C=
ENST00000636413.1:c.2870C=	ENSP00000490508.1:p.Ser957=
ENST00000636471.1:c.3281C=	ENSP00000490317.1:p.Ser1094=
ENST00000636732.2:c.*2923C=	ENSP00000490175.1:n.*2923C=
ENST00000636820.1:n.3306C=
ENST00000637045.1:c.2870C=	ENSP00000490141.1:p.Ser957=
ENST00000637304.1:c.2870C=	ENSP00000490872.1:p.Ser957=
ENST00000638007.1:c.2870C=	ENSP00000490723.1:p.Ser957=
ENST00000638087.1:c.2870C=	ENSP00000490673.1:p.Ser957=
ENST00000638128.1:c.2429C=	ENSP00000490934.1:p.Ser810=
ENST00000639389.1:c.151+6522C=	ENSP00000492572.1:n.151+6522C=
ENST00000647488.1:c.426C=	ENSP00000494820.1:n.426C=
ENST00000675069.1:c.737C=	ENSP00000502467.1:p.Ser246=
ENST00000303660.8:c.3203C=	ENSP00000302501.4:p.Ser1068=
ENST00000409487.7:c.3206C=	ENSP00000386854.2:p.Ser1069=
ENST00000419938.5:c.656-1008C=	ENSP00000394777.2:n.656-1008C=
ENST00000539609.7:c.3134C=	ENSP00000443792.2:p.Ser1045=
ENST00000558170.6:c.3206C=	ENSP00000454157.1:p.Ser1069=
ENST00000627532.2:c.3206C=	ENSP00000487174.1:p.Ser1069=
NM_001171653.1:c.3134C=	NP_001165124.1:p.Ser1045=
NM_014795.3:c.3206C=	NP_055610.1:p.Ser1069=
XM_006712881.2:c.3206C=	XP_006712944.1:p.Ser1069=
XM_006712882.2:c.3206C=	XP_006712945.1:p.Ser1069=
XM_011512231.1:c.3197C=	XP_011510533.1:p.Ser1066=
XM_011512232.1:c.3185C=	XP_011510534.1:p.Ser1062=
NM_014795.4:c.3206C= MANE Select	NP_055610.1:p.Ser1069=
NM_001171653.2:c.3134C=	NP_001165124.1:p.Ser1045=