Canonical Allele Identifier: CA1294881302
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389694G= , CM000664.2:g.144389694G= GRCh38
NC_000002.11:g.145147261G= , CM000664.1:g.145147261G= GRCh37
NC_000002.10:g.144863731G= NCBI36
NG_016431.1:g.135698C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3251C= ENSP00000508434.1:n.*3251C=
ENST00000440875.6:c.2625C= ENSP00000475553.3:p.Gly875=
ENST00000627532.3:c.3402C= MANE Select ENSP00000487174.1:p.Gly1134=
ENST00000636026.2:c.3290C= ENSP00000490776.1:p.Ala1097=
ENST00000636179.1:n.3371C=
ENST00000636413.1:c.3066C= ENSP00000490508.1:p.Gly1022=
ENST00000636471.1:c.3477C= ENSP00000490317.1:p.Gly1159=
ENST00000636732.2:c.*3119C= ENSP00000490175.1:n.*3119C=
ENST00000636820.1:n.3502C=
ENST00000637045.1:c.3066C= ENSP00000490141.1:p.Gly1022=
ENST00000637304.1:c.3066C= ENSP00000490872.1:p.Gly1022=
ENST00000638007.1:c.3066C= ENSP00000490723.1:p.Gly1022=
ENST00000638087.1:c.3066C= ENSP00000490673.1:p.Gly1022=
ENST00000638128.1:c.2625C= ENSP00000490934.1:p.Gly875=
ENST00000639389.1:c.151+6718C= ENSP00000492572.1:n.151+6718C=
ENST00000647488.1:c.622C= ENSP00000494820.1:n.622C=
ENST00000675069.1:c.933C= ENSP00000502467.1:p.Gly311=
ENST00000303660.8:c.3399C= ENSP00000302501.4:p.Gly1133=
ENST00000409487.7:c.3402C= ENSP00000386854.2:p.Gly1134=
ENST00000419938.5:c.656-812C= ENSP00000394777.2:n.656-812C=
ENST00000539609.7:c.3330C= ENSP00000443792.2:p.Gly1110=
ENST00000558170.6:c.3402C= ENSP00000454157.1:p.Gly1134=
ENST00000627532.2:c.3402C= ENSP00000487174.1:p.Gly1134=
NM_001171653.1:c.3330C= NP_001165124.1:p.Gly1110=
NM_014795.3:c.3402C= NP_055610.1:p.Gly1134=
XM_006712881.2:c.3402C= XP_006712944.1:p.Gly1134=
XM_006712882.2:c.3402C= XP_006712945.1:p.Gly1134=
XM_011512231.1:c.3393C= XP_011510533.1:p.Gly1131=
XM_011512232.1:c.3381C= XP_011510534.1:p.Gly1127=
NM_014795.4:c.3402C= MANE Select NP_055610.1:p.Gly1134=
NM_001171653.2:c.3330C= NP_001165124.1:p.Gly1110=