Canonical Allele Identifier: CA1294884889
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398429_144398430delinsGC , CM000664.2:g.144398429_144398430delinsGC GRCh38
NC_000002.11:g.145155996_145155997delinsGC , CM000664.1:g.145155996_145155997delinsGC GRCh37
NC_000002.10:g.144872466_144872467delinsGC NCBI36
NG_016431.1:g.126962_126963delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2606_*2607delinsGC ENSP00000508434.1:n.*2606_*2607delinsGC
ENST00000440875.6:c.1980_1981delinsGC ENSP00000475553.3:p.Gly660=
ENST00000627532.3:c.2757_2758delinsGC MANE Select ENSP00000487174.1:p.Gly919=
ENST00000636026.2:c.2757_2758delinsGC ENSP00000490776.1:p.Gly919=
ENST00000636179.1:n.2726_2727delinsGC
ENST00000636413.1:c.2421_2422delinsGC ENSP00000490508.1:p.Gly807=
ENST00000636471.1:c.2832_2833delinsGC ENSP00000490317.1:p.Gly944=
ENST00000636732.2:c.*2474_*2475delinsGC ENSP00000490175.1:n.*2474_*2475delinsGC
ENST00000636820.1:n.2857_2858delinsGC
ENST00000637045.1:c.2421_2422delinsGC ENSP00000490141.1:p.Gly807=
ENST00000637304.1:c.2421_2422delinsGC ENSP00000490872.1:p.Gly807=
ENST00000638007.1:c.2421_2422delinsGC ENSP00000490723.1:p.Gly807=
ENST00000638087.1:c.2421_2422delinsGC ENSP00000490673.1:p.Gly807=
ENST00000638128.1:c.1980_1981delinsGC ENSP00000490934.1:p.Gly660=
ENST00000675069.1:c.288_289delinsGC ENSP00000502467.1:p.Gly96=
ENST00000303660.8:c.2754_2755delinsGC ENSP00000302501.4:p.Gly918=
ENST00000409487.7:c.2757_2758delinsGC ENSP00000386854.2:p.Gly919=
ENST00000419938.5:c.655+2769_655+2770delinsGC ENSP00000394777.2:n.655+2769_655+2770delinsGC
ENST00000440875.5:c.1168-502_1168-501delinsGC ENSP00000475553.2:n.1168-502_1168-501delinsGC
ENST00000539609.7:c.2685_2686delinsGC ENSP00000443792.2:p.Gly895=
ENST00000558170.6:c.2757_2758delinsGC ENSP00000454157.1:p.Gly919=
ENST00000627532.2:c.2757_2758delinsGC ENSP00000487174.1:p.Gly919=
NM_001171653.1:c.2685_2686delinsGC NP_001165124.1:p.Gly895=
NM_014795.3:c.2757_2758delinsGC NP_055610.1:p.Gly919=
XM_006712881.2:c.2757_2758delinsGC XP_006712944.1:p.Gly919=
XM_006712882.2:c.2757_2758delinsGC XP_006712945.1:p.Gly919=
XM_011512231.1:c.2748_2749delinsGC XP_011510533.1:p.Gly916=
XM_011512232.1:c.2736_2737delinsGC XP_011510534.1:p.Gly912=
NM_014795.4:c.2757_2758delinsGC MANE Select NP_055610.1:p.Gly919=
NM_001171653.2:c.2685_2686delinsGC NP_001165124.1:p.Gly895=