Canonical Allele Identifier: CA1294881285

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389654A= , CM000664.2:g.144389654A=	GRCh38
NC_000002.11:g.145147221A= , CM000664.1:g.145147221A=	GRCh37
NC_000002.10:g.144863691A=	NCBI36
NG_016431.1:g.135738T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3291T=	ENSP00000508434.1:n.*3291T=
ENST00000440875.6:c.2665T=	ENSP00000475553.3:p.Tyr889=
ENST00000627532.3:c.3442T= MANE Select	ENSP00000487174.1:p.Tyr1148=
ENST00000636026.2:c.3330T=	ENSP00000490776.1:p.Ala1110=
ENST00000636179.1:n.3411T=
ENST00000636413.1:c.3106T=	ENSP00000490508.1:p.Tyr1036=
ENST00000636471.1:c.3517T=	ENSP00000490317.1:p.Tyr1173=
ENST00000636732.2:c.*3159T=	ENSP00000490175.1:n.*3159T=
ENST00000636820.1:n.3542T=
ENST00000637045.1:c.3106T=	ENSP00000490141.1:p.Tyr1036=
ENST00000637304.1:c.3106T=	ENSP00000490872.1:p.Tyr1036=
ENST00000638007.1:c.3106T=	ENSP00000490723.1:p.Tyr1036=
ENST00000638087.1:c.3106T=	ENSP00000490673.1:p.Tyr1036=
ENST00000638128.1:c.2665T=	ENSP00000490934.1:p.Tyr889=
ENST00000639389.1:c.151+6758T=	ENSP00000492572.1:n.151+6758T=
ENST00000647488.1:c.662T=	ENSP00000494820.1:n.662T=
ENST00000675069.1:c.973T=	ENSP00000502467.1:p.Tyr325=
ENST00000303660.8:c.3439T=	ENSP00000302501.4:p.Tyr1147=
ENST00000409487.7:c.3442T=	ENSP00000386854.2:p.Tyr1148=
ENST00000419938.5:c.656-772T=	ENSP00000394777.2:n.656-772T=
ENST00000539609.7:c.3370T=	ENSP00000443792.2:p.Tyr1124=
ENST00000558170.6:c.3442T=	ENSP00000454157.1:p.Tyr1148=
ENST00000627532.2:c.3442T=	ENSP00000487174.1:p.Tyr1148=
NM_001171653.1:c.3370T=	NP_001165124.1:p.Tyr1124=
NM_014795.3:c.3442T=	NP_055610.1:p.Tyr1148=
XM_006712881.2:c.3442T=	XP_006712944.1:p.Tyr1148=
XM_006712882.2:c.3442T=	XP_006712945.1:p.Tyr1148=
XM_011512231.1:c.3433T=	XP_011510533.1:p.Tyr1145=
XM_011512232.1:c.3421T=	XP_011510534.1:p.Tyr1141=
NM_014795.4:c.3442T= MANE Select	NP_055610.1:p.Tyr1148=
NM_001171653.2:c.3370T=	NP_001165124.1:p.Tyr1124=