Canonical Allele Identifier: CA2517152789

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389634_144389636del , CM000664.2:g.144389634_144389636del	GRCh38
NC_000002.11:g.145147201_145147203del , CM000664.1:g.145147201_145147203del	GRCh37
NC_000002.10:g.144863671_144863673del	NCBI36
NG_016431.1:g.135756_135758del

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3309_*3311del	ENSP00000508434.1:n.*3309_*3311del
ENST00000440875.6:c.2683_2685del	ENSP00000475553.3:p.Gln895del
ENST00000627532.3:c.3460_3462del MANE Select	ENSP00000487174.1:p.Gln1154del
ENST00000636026.2:c.3348_3350del	ENSP00000490776.1:p.Asp1116_Arg1117delins...
ENST00000636179.1:n.3429_3431del
ENST00000636413.1:c.3124_3126del	ENSP00000490508.1:p.Gln1042del
ENST00000636471.1:c.3535_3537del	ENSP00000490317.1:p.Gln1179del
ENST00000636732.2:c.*3177_*3179del	ENSP00000490175.1:n.*3177_*3179del
ENST00000636820.1:n.3560_3562del
ENST00000637045.1:c.3124_3126del	ENSP00000490141.1:p.Gln1042del
ENST00000637304.1:c.3124_3126del	ENSP00000490872.1:p.Gln1042del
ENST00000638007.1:c.3124_3126del	ENSP00000490723.1:p.Gln1042del
ENST00000638087.1:c.3124_3126del	ENSP00000490673.1:p.Gln1042del
ENST00000638128.1:c.2683_2685del	ENSP00000490934.1:p.Gln895del
ENST00000639389.1:c.151+6776_151+6778del	ENSP00000492572.1:n.151+6776_151+6778del
ENST00000647488.1:c.680_682del	ENSP00000494820.1:n.680_682del
ENST00000675069.1:c.991_993del	ENSP00000502467.1:p.Gln331del
ENST00000303660.8:c.3457_3459del	ENSP00000302501.4:p.Gln1153del
ENST00000409487.7:c.3460_3462del	ENSP00000386854.2:p.Gln1154del
ENST00000419938.5:c.656-754_656-752del	ENSP00000394777.2:n.656-754_656-752del
ENST00000539609.7:c.3388_3390del	ENSP00000443792.2:p.Gln1130del
ENST00000558170.6:c.3460_3462del	ENSP00000454157.1:p.Gln1154del
ENST00000627532.2:c.3460_3462del	ENSP00000487174.1:p.Gln1154del
NM_001171653.1:c.3388_3390del	NP_001165124.1:p.Gln1130del
NM_014795.3:c.3460_3462del	NP_055610.1:p.Gln1154del
XM_006712881.2:c.3460_3462del	XP_006712944.1:p.Gln1154del
XM_006712882.2:c.3460_3462del	XP_006712945.1:p.Gln1154del
XM_011512231.1:c.3451_3453del	XP_011510533.1:p.Gln1151del
XM_011512232.1:c.3439_3441del	XP_011510534.1:p.Gln1147del
NM_014795.4:c.3460_3462del MANE Select	NP_055610.1:p.Gln1154del
NM_001171653.2:c.3388_3390del	NP_001165124.1:p.Gln1130del