Canonical Allele Identifier: CA348699483
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2412983
ClinVar RCV Id: RCV003109998

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389731G>C , CM000664.2:g.144389731G>C GRCh38
NC_000002.11:g.145147298G>C , CM000664.1:g.145147298G>C GRCh37
NC_000002.10:g.144863768G>C NCBI36
NG_016431.1:g.135661C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3214C>G ENSP00000508434.1:n.*3214C>G
ENST00000440875.6:c.2588C>G ENSP00000475553.3:p.Ser863Cys
ENST00000627532.3:c.3365C>G MANE Select ENSP00000487174.1:p.Ser1122Cys
ENST00000636026.2:c.3253C>G ENSP00000490776.1:p.Leu1085Val
ENST00000636179.1:n.3334C>G
ENST00000636413.1:c.3029C>G ENSP00000490508.1:p.Ser1010Cys
ENST00000636471.1:c.3440C>G ENSP00000490317.1:p.Ser1147Cys
ENST00000636732.2:c.*3082C>G ENSP00000490175.1:n.*3082C>G
ENST00000636820.1:n.3465C>G
ENST00000637045.1:c.3029C>G ENSP00000490141.1:p.Ser1010Cys
ENST00000637304.1:c.3029C>G ENSP00000490872.1:p.Ser1010Cys
ENST00000638007.1:c.3029C>G ENSP00000490723.1:p.Ser1010Cys
ENST00000638087.1:c.3029C>G ENSP00000490673.1:p.Ser1010Cys
ENST00000638128.1:c.2588C>G ENSP00000490934.1:p.Ser863Cys
ENST00000639389.1:c.151+6681C>G ENSP00000492572.1:n.151+6681C>G
ENST00000647488.1:c.585C>G ENSP00000494820.1:n.585C>G
ENST00000675069.1:c.896C>G ENSP00000502467.1:p.Ser299Cys
ENST00000303660.8:c.3362C>G ENSP00000302501.4:p.Ser1121Cys
ENST00000409487.7:c.3365C>G ENSP00000386854.2:p.Ser1122Cys
ENST00000419938.5:c.656-849C>G ENSP00000394777.2:n.656-849C>G
ENST00000539609.7:c.3293C>G ENSP00000443792.2:p.Ser1098Cys
ENST00000558170.6:c.3365C>G ENSP00000454157.1:p.Ser1122Cys
ENST00000627532.2:c.3365C>G ENSP00000487174.1:p.Ser1122Cys
NM_001171653.1:c.3293C>G NP_001165124.1:p.Ser1098Cys
NM_014795.3:c.3365C>G NP_055610.1:p.Ser1122Cys
XM_006712881.2:c.3365C>G XP_006712944.1:p.Ser1122Cys
XM_006712882.2:c.3365C>G XP_006712945.1:p.Ser1122Cys
XM_011512231.1:c.3356C>G XP_011510533.1:p.Ser1119Cys
XM_011512232.1:c.3344C>G XP_011510534.1:p.Ser1115Cys
NM_014795.4:c.3365C>G MANE Select NP_055610.1:p.Ser1122Cys
NM_001171653.2:c.3293C>G NP_001165124.1:p.Ser1098Cys