Canonical Allele Identifier: CA297617
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181745
ClinVar RCV Id: RCV000159485
dbSNP Id: rs730881202

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389966C>T , CM000664.2:g.144389966C>T GRCh38
NC_000002.11:g.145147533C>T , CM000664.1:g.145147533C>T GRCh37
NC_000002.10:g.144864003C>T NCBI36
NG_016431.1:g.135426G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2979G>A ENSP00000508434.1:n.*2979G>A
ENST00000440875.6:c.2353G>A ENSP00000475553.3:p.Glu785Lys
ENST00000627532.3:c.3130G>A MANE Select ENSP00000487174.1:p.Glu1044Lys
ENST00000636026.2:c.3130G>A ENSP00000490776.1:p.Glu1044Lys
ENST00000636179.1:n.3099G>A
ENST00000636413.1:c.2794G>A ENSP00000490508.1:p.Glu932Lys
ENST00000636471.1:c.3205G>A ENSP00000490317.1:p.Glu1069Lys
ENST00000636732.2:c.*2847G>A ENSP00000490175.1:n.*2847G>A
ENST00000636820.1:n.3230G>A
ENST00000637045.1:c.2794G>A ENSP00000490141.1:p.Glu932Lys
ENST00000637304.1:c.2794G>A ENSP00000490872.1:p.Glu932Lys
ENST00000638007.1:c.2794G>A ENSP00000490723.1:p.Glu932Lys
ENST00000638087.1:c.2794G>A ENSP00000490673.1:p.Glu932Lys
ENST00000638128.1:c.2353G>A ENSP00000490934.1:p.Glu785Lys
ENST00000639389.1:c.151+6446G>A ENSP00000492572.1:n.151+6446G>A
ENST00000647488.1:c.350G>A ENSP00000494820.1:n.350G>A
ENST00000675069.1:c.661G>A ENSP00000502467.1:p.Glu221Lys
ENST00000303660.8:c.3127G>A ENSP00000302501.4:p.Glu1043Lys
ENST00000409487.7:c.3130G>A ENSP00000386854.2:p.Glu1044Lys
ENST00000419938.5:c.656-1084G>A ENSP00000394777.2:n.656-1084G>A
ENST00000539609.7:c.3058G>A ENSP00000443792.2:p.Glu1020Lys
ENST00000558170.6:c.3130G>A ENSP00000454157.1:p.Glu1044Lys
ENST00000627532.2:c.3130G>A ENSP00000487174.1:p.Glu1044Lys
NM_001171653.1:c.3058G>A NP_001165124.1:p.Glu1020Lys
NM_014795.3:c.3130G>A NP_055610.1:p.Glu1044Lys
XM_006712881.2:c.3130G>A XP_006712944.1:p.Glu1044Lys
XM_006712882.2:c.3130G>A XP_006712945.1:p.Glu1044Lys
XM_011512231.1:c.3121G>A XP_011510533.1:p.Glu1041Lys
XM_011512232.1:c.3109G>A XP_011510534.1:p.Glu1037Lys
NM_014795.4:c.3130G>A MANE Select NP_055610.1:p.Glu1044Lys
NM_001171653.2:c.3058G>A NP_001165124.1:p.Glu1020Lys