Canonical Allele Identifier: CA658795856

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 500047
• ClinVar RCV Id: RCV000594850
• dbSNP Id: rs1553961343
• MyVariant Identifiers: chr2:g.145154059_145154060del (hg19) ; chr2:g.144396492_144396493del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396496_144396497del , CM000664.2:g.144396496_144396497del	GRCh38
NC_000002.11:g.145154063_145154064del , CM000664.1:g.145154063_145154064del	GRCh37
NC_000002.10:g.144870533_144870534del	NCBI36
NG_016431.1:g.128899_128900del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2835_*2836del	ENSP00000508434.1:n.*2835_*2836del
ENST00000440875.6:c.2209_2210del	ENSP00000475553.3:p.Ser737TrpfsTer6
ENST00000627532.3:c.2986_2987del MANE Select	ENSP00000487174.1:p.Ser996TrpfsTer6
ENST00000636026.2:c.2986_2987del	ENSP00000490776.1:p.Ser996TrpfsTer6
ENST00000636179.1:n.2955_2956del
ENST00000636413.1:c.2650_2651del	ENSP00000490508.1:p.Ser884TrpfsTer6
ENST00000636471.1:c.3061_3062del	ENSP00000490317.1:p.Ser1021TrpfsTer6
ENST00000636732.2:c.*2703_*2704del	ENSP00000490175.1:n.*2703_*2704del
ENST00000636820.1:n.3086_3087del
ENST00000637045.1:c.2650_2651del	ENSP00000490141.1:p.Ser884TrpfsTer6
ENST00000637304.1:c.2650_2651del	ENSP00000490872.1:p.Ser884TrpfsTer6
ENST00000638007.1:c.2650_2651del	ENSP00000490723.1:p.Ser884TrpfsTer6
ENST00000638087.1:c.2650_2651del	ENSP00000490673.1:p.Ser884TrpfsTer6
ENST00000638128.1:c.2209_2210del	ENSP00000490934.1:p.Ser737TrpfsTer6
ENST00000639389.1:c.70_71del	ENSP00000492572.1:p.Ser24TrpfsTer6
ENST00000647488.1:c.118_119del	ENSP00000494820.1:p.Ser40TrpfsTer6
ENST00000675069.1:c.517_518del	ENSP00000502467.1:p.Ser173TrpfsTer6
ENST00000303660.8:c.2983_2984del	ENSP00000302501.4:p.Ser995TrpfsTer6
ENST00000409487.7:c.2986_2987del	ENSP00000386854.2:p.Ser996TrpfsTer6
ENST00000419938.5:c.655+4706_655+4707del	ENSP00000394777.2:n.655+4706_655+4707del
ENST00000539609.7:c.2914_2915del	ENSP00000443792.2:p.Ser972TrpfsTer6
ENST00000558170.6:c.2986_2987del	ENSP00000454157.1:p.Ser996TrpfsTer6
ENST00000627532.2:c.2986_2987del	ENSP00000487174.1:p.Ser996TrpfsTer6
NM_001171653.1:c.2914_2915del	NP_001165124.1:p.Ser972TrpfsTer6
NM_014795.3:c.2986_2987del	NP_055610.1:p.Ser996TrpfsTer6
XM_006712881.2:c.2986_2987del	XP_006712944.1:p.Ser996TrpfsTer6
XM_006712882.2:c.2986_2987del	XP_006712945.1:p.Ser996TrpfsTer6
XM_011512231.1:c.2977_2978del	XP_011510533.1:p.Ser993TrpfsTer6
XM_011512232.1:c.2965_2966del	XP_011510534.1:p.Ser989TrpfsTer6
NM_014795.4:c.2986_2987del MANE Select	NP_055610.1:p.Ser996TrpfsTer6
NM_001171653.2:c.2914_2915del	NP_001165124.1:p.Ser972TrpfsTer6