Canonical Allele Identifier: CA348712350
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399979A>C , CM000664.2:g.144399979A>C GRCh38
NC_000002.11:g.145157546A>C , CM000664.1:g.145157546A>C GRCh37
NC_000002.10:g.144874016A>C NCBI36
NG_016431.1:g.125413T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1057T>G ENSP00000508434.1:n.*1057T>G
ENST00000440875.6:c.431T>G ENSP00000475553.3:p.Leu144Arg
ENST00000627532.3:c.1208T>G MANE Select ENSP00000487174.1:p.Leu403Arg
ENST00000636026.2:c.1208T>G ENSP00000490776.1:p.Leu403Arg
ENST00000636179.1:n.1177T>G
ENST00000636413.1:c.872T>G ENSP00000490508.1:p.Leu291Arg
ENST00000636471.1:c.1283T>G ENSP00000490317.1:p.Leu428Arg
ENST00000636732.2:c.*925T>G ENSP00000490175.1:n.*925T>G
ENST00000636820.1:n.1308T>G
ENST00000637045.1:c.872T>G ENSP00000490141.1:p.Leu291Arg
ENST00000637267.2:c.1208T>G ENSP00000490293.2:p.Leu403Arg
ENST00000637304.1:c.872T>G ENSP00000490872.1:p.Leu291Arg
ENST00000638007.1:c.872T>G ENSP00000490723.1:p.Leu291Arg
ENST00000638087.1:c.872T>G ENSP00000490673.1:p.Leu291Arg
ENST00000638128.1:c.431T>G ENSP00000490934.1:p.Leu144Arg
ENST00000675069.1:c.-133-1129T>G ENSP00000502467.1:n.-133-1129T>G
ENST00000675145.1:n.1756T>G
ENST00000303660.8:c.1205T>G ENSP00000302501.4:p.Leu402Arg
ENST00000392861.6:c.1292T>G ENSP00000376601.3:p.Leu431Arg
ENST00000409487.7:c.1208T>G ENSP00000386854.2:p.Leu403Arg
ENST00000419938.5:c.655+1220T>G ENSP00000394777.2:n.655+1220T>G
ENST00000427902.5:c.1295T>G ENSP00000395496.2:p.Leu432Arg
ENST00000440875.5:c.1153+40T>G ENSP00000475553.2:n.1153+40T>G
ENST00000539609.7:c.1136T>G ENSP00000443792.2:p.Leu379Arg
ENST00000558170.6:c.1208T>G ENSP00000454157.1:p.Leu403Arg
ENST00000627532.2:c.1208T>G ENSP00000487174.1:p.Leu403Arg
NM_001171653.1:c.1136T>G NP_001165124.1:p.Leu379Arg
NM_014795.3:c.1208T>G NP_055610.1:p.Leu403Arg
XM_006712881.2:c.1208T>G XP_006712944.1:p.Leu403Arg
XM_006712882.2:c.1208T>G XP_006712945.1:p.Leu403Arg
XM_011512231.1:c.1199T>G XP_011510533.1:p.Leu400Arg
XM_011512232.1:c.1187T>G XP_011510534.1:p.Leu396Arg
NM_014795.4:c.1208T>G MANE Select NP_055610.1:p.Leu403Arg
NM_001171653.2:c.1136T>G NP_001165124.1:p.Leu379Arg