Canonical Allele Identifier: CA348714775
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144404015C>A , CM000664.2:g.144404015C>A GRCh38
NC_000002.11:g.145161582C>A , CM000664.1:g.145161582C>A GRCh37
NC_000002.10:g.144878052C>A NCBI36
NG_016431.1:g.121377G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*557G>T ENSP00000508434.1:n.*557G>T
ENST00000440875.6:c.-70G>T ENSP00000475553.3:n.-70G>T
ENST00000627532.3:c.708G>T MANE Select ENSP00000487174.1:p.Lys236Asn
ENST00000636026.2:c.708G>T ENSP00000490776.1:p.Lys236Asn
ENST00000636179.1:n.677G>T
ENST00000636413.1:c.372G>T ENSP00000490508.1:p.Lys124Asn
ENST00000636471.1:c.708G>T ENSP00000490317.1:p.Lys236Asn
ENST00000636732.2:c.*425G>T ENSP00000490175.1:n.*425G>T
ENST00000636820.1:n.808G>T
ENST00000637045.1:c.372G>T ENSP00000490141.1:p.Lys124Asn
ENST00000637267.2:c.708G>T ENSP00000490293.2:p.Lys236Asn
ENST00000637304.1:c.372G>T ENSP00000490872.1:p.Lys124Asn
ENST00000638007.1:c.372G>T ENSP00000490723.1:p.Lys124Asn
ENST00000638087.1:c.372G>T ENSP00000490673.1:p.Lys124Asn
ENST00000638128.1:c.-70G>T ENSP00000490934.1:n.-70G>T
ENST00000675069.1:c.-133-5165G>T ENSP00000502467.1:n.-133-5165G>T
ENST00000303660.8:c.705G>T ENSP00000302501.4:p.Lys235Asn
ENST00000392861.6:c.792G>T ENSP00000376601.3:p.Lys264Asn
ENST00000409487.7:c.708G>T ENSP00000386854.2:p.Lys236Asn
ENST00000419938.5:c.447G>T ENSP00000394777.2:p.Lys149Asn
ENST00000427902.5:c.795G>T ENSP00000395496.2:p.Lys265Asn
ENST00000440875.5:c.693G>T ENSP00000475553.2:p.Lys231Asn
ENST00000497268.1:n.654G>T
ENST00000539609.7:c.636G>T ENSP00000443792.2:p.Lys212Asn
ENST00000558170.6:c.708G>T ENSP00000454157.1:p.Lys236Asn
ENST00000627532.2:c.708G>T ENSP00000487174.1:p.Lys236Asn
NM_001171653.1:c.636G>T NP_001165124.1:p.Lys212Asn
NM_014795.3:c.708G>T NP_055610.1:p.Lys236Asn
XM_006712881.2:c.708G>T XP_006712944.1:p.Lys236Asn
XM_006712882.2:c.708G>T XP_006712945.1:p.Lys236Asn
XM_011512231.1:c.699G>T XP_011510533.1:p.Lys233Asn
XM_011512232.1:c.687G>T XP_011510534.1:p.Lys229Asn
NM_014795.4:c.708G>T MANE Select NP_055610.1:p.Lys236Asn
NM_001171653.2:c.636G>T NP_001165124.1:p.Lys212Asn