Canonical Allele Identifier: CA1294884883

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398420A= , CM000664.2:g.144398420A=	GRCh38
NC_000002.11:g.145155987A= , CM000664.1:g.145155987A=	GRCh37
NC_000002.10:g.144872457A=	NCBI36
NG_016431.1:g.126972T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2616T=	ENSP00000508434.1:n.*2616T=
ENST00000440875.6:c.1990T=	ENSP00000475553.3:p.Tyr664=
ENST00000627532.3:c.2767T= MANE Select	ENSP00000487174.1:p.Tyr923=
ENST00000636026.2:c.2767T=	ENSP00000490776.1:p.Tyr923=
ENST00000636179.1:n.2736T=
ENST00000636413.1:c.2431T=	ENSP00000490508.1:p.Tyr811=
ENST00000636471.1:c.2842T=	ENSP00000490317.1:p.Tyr948=
ENST00000636732.2:c.*2484T=	ENSP00000490175.1:n.*2484T=
ENST00000636820.1:n.2867T=
ENST00000637045.1:c.2431T=	ENSP00000490141.1:p.Tyr811=
ENST00000637304.1:c.2431T=	ENSP00000490872.1:p.Tyr811=
ENST00000638007.1:c.2431T=	ENSP00000490723.1:p.Tyr811=
ENST00000638087.1:c.2431T=	ENSP00000490673.1:p.Tyr811=
ENST00000638128.1:c.1990T=	ENSP00000490934.1:p.Tyr664=
ENST00000675069.1:c.298T=	ENSP00000502467.1:p.Tyr100=
ENST00000303660.8:c.2764T=	ENSP00000302501.4:p.Tyr922=
ENST00000409487.7:c.2767T=	ENSP00000386854.2:p.Tyr923=
ENST00000419938.5:c.655+2779T=	ENSP00000394777.2:n.655+2779T=
ENST00000440875.5:c.1168-492T=	ENSP00000475553.2:n.1168-492T=
ENST00000539609.7:c.2695T=	ENSP00000443792.2:p.Tyr899=
ENST00000558170.6:c.2767T=	ENSP00000454157.1:p.Tyr923=
ENST00000627532.2:c.2767T=	ENSP00000487174.1:p.Tyr923=
NM_001171653.1:c.2695T=	NP_001165124.1:p.Tyr899=
NM_014795.3:c.2767T=	NP_055610.1:p.Tyr923=
XM_006712881.2:c.2767T=	XP_006712944.1:p.Tyr923=
XM_006712882.2:c.2767T=	XP_006712945.1:p.Tyr923=
XM_011512231.1:c.2758T=	XP_011510533.1:p.Tyr920=
XM_011512232.1:c.2746T=	XP_011510534.1:p.Tyr916=
NM_014795.4:c.2767T= MANE Select	NP_055610.1:p.Tyr923=
NM_001171653.2:c.2695T=	NP_001165124.1:p.Tyr899=