Canonical Allele Identifier: CA429441179

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147307delT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389740del , CM000664.2:g.144389740del	GRCh38
NC_000002.11:g.145147307del , CM000664.1:g.145147307del	GRCh37
NC_000002.10:g.144863777del	NCBI36
NG_016431.1:g.135652del

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3205del	ENSP00000508434.1:n.*3205del
ENST00000440875.6:c.2579del	ENSP00000475553.3:p.Gln860ArgfsTer?
ENST00000627532.3:c.3356del MANE Select	ENSP00000487174.1:p.Gln1119ArgfsTer?
ENST00000636026.2:c.3244del	ENSP00000490776.1:p.Arg1082GlyfsTer4
ENST00000636179.1:n.3325del
ENST00000636413.1:c.3020del	ENSP00000490508.1:p.Gln1007ArgfsTer?
ENST00000636471.1:c.3431del	ENSP00000490317.1:p.Gln1144ArgfsTer?
ENST00000636732.2:c.*3073del	ENSP00000490175.1:n.*3073del
ENST00000636820.1:n.3456del
ENST00000637045.1:c.3020del	ENSP00000490141.1:p.Gln1007ArgfsTer?
ENST00000637304.1:c.3020del	ENSP00000490872.1:p.Gln1007ArgfsTer?
ENST00000638007.1:c.3020del	ENSP00000490723.1:p.Gln1007ArgfsTer?
ENST00000638087.1:c.3020del	ENSP00000490673.1:p.Gln1007ArgfsTer?
ENST00000638128.1:c.2579del	ENSP00000490934.1:p.Gln860ArgfsTer?
ENST00000639389.1:c.151+6672del	ENSP00000492572.1:n.151+6672del
ENST00000647488.1:c.576del	ENSP00000494820.1:n.576del
ENST00000675069.1:c.887del	ENSP00000502467.1:p.Gln296ArgfsTer?
ENST00000303660.8:c.3353del	ENSP00000302501.4:p.Gln1118ArgfsTer?
ENST00000409487.7:c.3356del	ENSP00000386854.2:p.Gln1119ArgfsTer?
ENST00000419938.5:c.656-858del	ENSP00000394777.2:n.656-858del
ENST00000539609.7:c.3284del	ENSP00000443792.2:p.Gln1095ArgfsTer?
ENST00000558170.6:c.3356del	ENSP00000454157.1:p.Gln1119ArgfsTer?
ENST00000627532.2:c.3356del	ENSP00000487174.1:p.Gln1119ArgfsTer?
NM_001171653.1:c.3284del	NP_001165124.1:p.Gln1095ArgfsTer?
NM_014795.3:c.3356del	NP_055610.1:p.Gln1119ArgfsTer?
XM_006712881.2:c.3356del	XP_006712944.1:p.Gln1119ArgfsTer?
XM_006712882.2:c.3356del	XP_006712945.1:p.Gln1119ArgfsTer?
XM_011512231.1:c.3347del	XP_011510533.1:p.Gln1116ArgfsTer?
XM_011512232.1:c.3335del	XP_011510534.1:p.Gln1112ArgfsTer?
NM_014795.4:c.3356del MANE Select	NP_055610.1:p.Gln1119ArgfsTer?
NM_001171653.2:c.3284del	NP_001165124.1:p.Gln1095ArgfsTer?