Canonical Allele Identifier: CA148686

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144400257G>A , CM000664.2:g.144400257G>A	GRCh38
NC_000002.11:g.145157824G>A , CM000664.1:g.145157824G>A	GRCh37
NC_000002.10:g.144874294G>A	NCBI36
NG_016431.1:g.125135C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*779C>T	ENSP00000508434.1:n.*779C>T
ENST00000440875.6:c.153C>T	ENSP00000475553.3:p.Tyr51=
ENST00000627532.3:c.930C>T MANE Select	ENSP00000487174.1:p.Tyr310=
ENST00000636026.2:c.930C>T	ENSP00000490776.1:p.Tyr310=
ENST00000636179.1:n.899C>T
ENST00000636413.1:c.594C>T	ENSP00000490508.1:p.Tyr198=
ENST00000636471.1:c.1005C>T	ENSP00000490317.1:p.Tyr335=
ENST00000636732.2:c.*647C>T	ENSP00000490175.1:n.*647C>T
ENST00000636820.1:n.1030C>T
ENST00000637045.1:c.594C>T	ENSP00000490141.1:p.Tyr198=
ENST00000637267.2:c.930C>T	ENSP00000490293.2:p.Tyr310=
ENST00000637304.1:c.594C>T	ENSP00000490872.1:p.Tyr198=
ENST00000638007.1:c.594C>T	ENSP00000490723.1:p.Tyr198=
ENST00000638087.1:c.594C>T	ENSP00000490673.1:p.Tyr198=
ENST00000638128.1:c.153C>T	ENSP00000490934.1:p.Tyr51=
ENST00000675069.1:c.-133-1407C>T	ENSP00000502467.1:n.-133-1407C>T
ENST00000675145.1:n.1478C>T
ENST00000303660.8:c.927C>T	ENSP00000302501.4:p.Tyr309=
ENST00000392861.6:c.1014C>T	ENSP00000376601.3:p.Tyr338=
ENST00000409487.7:c.930C>T	ENSP00000386854.2:p.Tyr310=
ENST00000419938.5:c.655+942C>T	ENSP00000394777.2:n.655+942C>T
ENST00000427902.5:c.1017C>T	ENSP00000395496.2:p.Tyr339=
ENST00000440875.5:c.915C>T	ENSP00000475553.2:p.Tyr305=
ENST00000539609.7:c.858C>T	ENSP00000443792.2:p.Tyr286=
ENST00000558170.6:c.930C>T	ENSP00000454157.1:p.Tyr310=
ENST00000627532.2:c.930C>T	ENSP00000487174.1:p.Tyr310=
NM_001171653.1:c.858C>T	NP_001165124.1:p.Tyr286=
NM_014795.3:c.930C>T	NP_055610.1:p.Tyr310=
XM_006712881.2:c.930C>T	XP_006712944.1:p.Tyr310=
XM_006712882.2:c.930C>T	XP_006712945.1:p.Tyr310=
XM_011512231.1:c.921C>T	XP_011510533.1:p.Tyr307=
XM_011512232.1:c.909C>T	XP_011510534.1:p.Tyr303=
NM_014795.4:c.930C>T MANE Select	NP_055610.1:p.Tyr310=
NM_001171653.2:c.858C>T	NP_001165124.1:p.Tyr286=