Canonical Allele Identifier: CA348706606
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398336G>T , CM000664.2:g.144398336G>T GRCh38
NC_000002.11:g.145155903G>T , CM000664.1:g.145155903G>T GRCh37
NC_000002.10:g.144872373G>T NCBI36
NG_016431.1:g.127056C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2700C>A ENSP00000508434.1:n.*2700C>A
ENST00000440875.6:c.2074C>A ENSP00000475553.3:p.Gln692Lys
ENST00000627532.3:c.2851C>A MANE Select ENSP00000487174.1:p.Gln951Lys
ENST00000636026.2:c.2851C>A ENSP00000490776.1:p.Gln951Lys
ENST00000636179.1:n.2820C>A
ENST00000636413.1:c.2515C>A ENSP00000490508.1:p.Gln839Lys
ENST00000636471.1:c.2926C>A ENSP00000490317.1:p.Gln976Lys
ENST00000636732.2:c.*2568C>A ENSP00000490175.1:n.*2568C>A
ENST00000636820.1:n.2951C>A
ENST00000637045.1:c.2515C>A ENSP00000490141.1:p.Gln839Lys
ENST00000637304.1:c.2515C>A ENSP00000490872.1:p.Gln839Lys
ENST00000638007.1:c.2515C>A ENSP00000490723.1:p.Gln839Lys
ENST00000638087.1:c.2515C>A ENSP00000490673.1:p.Gln839Lys
ENST00000638128.1:c.2074C>A ENSP00000490934.1:p.Gln692Lys
ENST00000675069.1:c.382C>A ENSP00000502467.1:p.Gln128Lys
ENST00000303660.8:c.2848C>A ENSP00000302501.4:p.Gln950Lys
ENST00000409487.7:c.2851C>A ENSP00000386854.2:p.Gln951Lys
ENST00000419938.5:c.655+2863C>A ENSP00000394777.2:n.655+2863C>A
ENST00000440875.5:c.1168-408C>A ENSP00000475553.2:n.1168-408C>A
ENST00000539609.7:c.2779C>A ENSP00000443792.2:p.Gln927Lys
ENST00000558170.6:c.2851C>A ENSP00000454157.1:p.Gln951Lys
ENST00000627532.2:c.2851C>A ENSP00000487174.1:p.Gln951Lys
NM_001171653.1:c.2779C>A NP_001165124.1:p.Gln927Lys
NM_014795.3:c.2851C>A NP_055610.1:p.Gln951Lys
XM_006712881.2:c.2851C>A XP_006712944.1:p.Gln951Lys
XM_006712882.2:c.2851C>A XP_006712945.1:p.Gln951Lys
XM_011512231.1:c.2842C>A XP_011510533.1:p.Gln948Lys
XM_011512232.1:c.2830C>A XP_011510534.1:p.Gln944Lys
NM_014795.4:c.2851C>A MANE Select NP_055610.1:p.Gln951Lys
NM_001171653.2:c.2779C>A NP_001165124.1:p.Gln927Lys