Canonical Allele Identifier: CA429444972

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145155885G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398318G>T , CM000664.2:g.144398318G>T	GRCh38
NC_000002.11:g.145155885G>T , CM000664.1:g.145155885G>T	GRCh37
NC_000002.10:g.144872355G>T	NCBI36
NG_016431.1:g.127074C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2718C>A	ENSP00000508434.1:n.*2718C>A
ENST00000440875.6:c.2092C>A	ENSP00000475553.3:p.Arg698=
ENST00000627532.3:c.2869C>A MANE Select	ENSP00000487174.1:p.Arg957=
ENST00000636026.2:c.2869C>A	ENSP00000490776.1:p.Arg957=
ENST00000636179.1:n.2838C>A
ENST00000636413.1:c.2533C>A	ENSP00000490508.1:p.Arg845=
ENST00000636471.1:c.2944C>A	ENSP00000490317.1:p.Arg982=
ENST00000636732.2:c.*2586C>A	ENSP00000490175.1:n.*2586C>A
ENST00000636820.1:n.2969C>A
ENST00000637045.1:c.2533C>A	ENSP00000490141.1:p.Arg845=
ENST00000637304.1:c.2533C>A	ENSP00000490872.1:p.Arg845=
ENST00000638007.1:c.2533C>A	ENSP00000490723.1:p.Arg845=
ENST00000638087.1:c.2533C>A	ENSP00000490673.1:p.Arg845=
ENST00000638128.1:c.2092C>A	ENSP00000490934.1:p.Arg698=
ENST00000647488.1:c.1C>A	ENSP00000494820.1:p.Arg1=
ENST00000675069.1:c.400C>A	ENSP00000502467.1:p.Arg134=
ENST00000303660.8:c.2866C>A	ENSP00000302501.4:p.Arg956=
ENST00000409487.7:c.2869C>A	ENSP00000386854.2:p.Arg957=
ENST00000419938.5:c.655+2881C>A	ENSP00000394777.2:n.655+2881C>A
ENST00000440875.5:c.1168-390C>A	ENSP00000475553.2:n.1168-390C>A
ENST00000539609.7:c.2797C>A	ENSP00000443792.2:p.Arg933=
ENST00000558170.6:c.2869C>A	ENSP00000454157.1:p.Arg957=
ENST00000627532.2:c.2869C>A	ENSP00000487174.1:p.Arg957=
NM_001171653.1:c.2797C>A	NP_001165124.1:p.Arg933=
NM_014795.3:c.2869C>A	NP_055610.1:p.Arg957=
XM_006712881.2:c.2869C>A	XP_006712944.1:p.Arg957=
XM_006712882.2:c.2869C>A	XP_006712945.1:p.Arg957=
XM_011512231.1:c.2860C>A	XP_011510533.1:p.Arg954=
XM_011512232.1:c.2848C>A	XP_011510534.1:p.Arg950=
NM_014795.4:c.2869C>A MANE Select	NP_055610.1:p.Arg957=
NM_001171653.2:c.2797C>A	NP_001165124.1:p.Arg933=