Canonical Allele Identifier: CA348712365
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399985T>C , CM000664.2:g.144399985T>C GRCh38
NC_000002.11:g.145157552T>C , CM000664.1:g.145157552T>C GRCh37
NC_000002.10:g.144874022T>C NCBI36
NG_016431.1:g.125407A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1051A>G ENSP00000508434.1:n.*1051A>G
ENST00000440875.6:c.425A>G ENSP00000475553.3:p.Lys142Arg
ENST00000627532.3:c.1202A>G MANE Select ENSP00000487174.1:p.Lys401Arg
ENST00000636026.2:c.1202A>G ENSP00000490776.1:p.Lys401Arg
ENST00000636179.1:n.1171A>G
ENST00000636413.1:c.866A>G ENSP00000490508.1:p.Lys289Arg
ENST00000636471.1:c.1277A>G ENSP00000490317.1:p.Lys426Arg
ENST00000636732.2:c.*919A>G ENSP00000490175.1:n.*919A>G
ENST00000636820.1:n.1302A>G
ENST00000637045.1:c.866A>G ENSP00000490141.1:p.Lys289Arg
ENST00000637267.2:c.1202A>G ENSP00000490293.2:p.Lys401Arg
ENST00000637304.1:c.866A>G ENSP00000490872.1:p.Lys289Arg
ENST00000638007.1:c.866A>G ENSP00000490723.1:p.Lys289Arg
ENST00000638087.1:c.866A>G ENSP00000490673.1:p.Lys289Arg
ENST00000638128.1:c.425A>G ENSP00000490934.1:p.Lys142Arg
ENST00000675069.1:c.-133-1135A>G ENSP00000502467.1:n.-133-1135A>G
ENST00000675145.1:n.1750A>G
ENST00000303660.8:c.1199A>G ENSP00000302501.4:p.Lys400Arg
ENST00000392861.6:c.1286A>G ENSP00000376601.3:p.Lys429Arg
ENST00000409487.7:c.1202A>G ENSP00000386854.2:p.Lys401Arg
ENST00000419938.5:c.655+1214A>G ENSP00000394777.2:n.655+1214A>G
ENST00000427902.5:c.1289A>G ENSP00000395496.2:p.Lys430Arg
ENST00000440875.5:c.1153+34A>G ENSP00000475553.2:n.1153+34A>G
ENST00000539609.7:c.1130A>G ENSP00000443792.2:p.Lys377Arg
ENST00000558170.6:c.1202A>G ENSP00000454157.1:p.Lys401Arg
ENST00000627532.2:c.1202A>G ENSP00000487174.1:p.Lys401Arg
NM_001171653.1:c.1130A>G NP_001165124.1:p.Lys377Arg
NM_014795.3:c.1202A>G NP_055610.1:p.Lys401Arg
XM_006712881.2:c.1202A>G XP_006712944.1:p.Lys401Arg
XM_006712882.2:c.1202A>G XP_006712945.1:p.Lys401Arg
XM_011512231.1:c.1193A>G XP_011510533.1:p.Lys398Arg
XM_011512232.1:c.1181A>G XP_011510534.1:p.Lys394Arg
NM_014795.4:c.1202A>G MANE Select NP_055610.1:p.Lys401Arg
NM_001171653.2:c.1130A>G NP_001165124.1:p.Lys377Arg