Canonical Allele Identifier: CA1294885040

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398821_144398822delinsGA , CM000664.2:g.144398821_144398822delinsGA	GRCh38
NC_000002.11:g.145156388_145156389delinsGA , CM000664.1:g.145156388_145156389delinsGA	GRCh37
NC_000002.10:g.144872858_144872859delinsGA	NCBI36
NG_016431.1:g.126570_126571delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2214_*2215delinsTC	ENSP00000508434.1:n.*2214_*2215delinsTC
ENST00000440875.6:c.1588_1589delinsTC	ENSP00000475553.3:p.Ser530=
ENST00000627532.3:c.2365_2366delinsTC MANE Select	ENSP00000487174.1:p.Ser789=
ENST00000636026.2:c.2365_2366delinsTC	ENSP00000490776.1:p.Ser789=
ENST00000636179.1:n.2334_2335delinsTC
ENST00000636413.1:c.2029_2030delinsTC	ENSP00000490508.1:p.Ser677=
ENST00000636471.1:c.2440_2441delinsTC	ENSP00000490317.1:p.Ser814=
ENST00000636732.2:c.*2082_*2083delinsTC	ENSP00000490175.1:n.*2082_*2083delinsTC
ENST00000636820.1:n.2465_2466delinsTC
ENST00000637045.1:c.2029_2030delinsTC	ENSP00000490141.1:p.Ser677=
ENST00000637304.1:c.2029_2030delinsTC	ENSP00000490872.1:p.Ser677=
ENST00000638007.1:c.2029_2030delinsTC	ENSP00000490723.1:p.Ser677=
ENST00000638087.1:c.2029_2030delinsTC	ENSP00000490673.1:p.Ser677=
ENST00000638128.1:c.1588_1589delinsTC	ENSP00000490934.1:p.Ser530=
ENST00000675069.1:c.-105_-104delinsTC	ENSP00000502467.1:n.-105_-104delinsTC
ENST00000675145.1:n.2913_2914delinsTC
ENST00000303660.8:c.2362_2363delinsTC	ENSP00000302501.4:p.Ser788=
ENST00000409487.7:c.2365_2366delinsTC	ENSP00000386854.2:p.Ser789=
ENST00000419938.5:c.655+2377_655+2378delinsTC	ENSP00000394777.2:n.655+2377_655+2378delinsTC
ENST00000440875.5:c.1167+715_1167+716delinsTC	ENSP00000475553.2:n.1167+715_1167+716delinsTC
ENST00000539609.7:c.2293_2294delinsTC	ENSP00000443792.2:p.Ser765=
ENST00000558170.6:c.2365_2366delinsTC	ENSP00000454157.1:p.Ser789=
ENST00000627532.2:c.2365_2366delinsTC	ENSP00000487174.1:p.Ser789=
NM_001171653.1:c.2293_2294delinsTC	NP_001165124.1:p.Ser765=
NM_014795.3:c.2365_2366delinsTC	NP_055610.1:p.Ser789=
XM_006712881.2:c.2365_2366delinsTC	XP_006712944.1:p.Ser789=
XM_006712882.2:c.2365_2366delinsTC	XP_006712945.1:p.Ser789=
XM_011512231.1:c.2356_2357delinsTC	XP_011510533.1:p.Ser786=
XM_011512232.1:c.2344_2345delinsTC	XP_011510534.1:p.Ser782=
NM_014795.4:c.2365_2366delinsTC MANE Select	NP_055610.1:p.Ser789=
NM_001171653.2:c.2293_2294delinsTC	NP_001165124.1:p.Ser765=