Canonical Allele Identifier: CA1294885033

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398807_144398810delinsTAGA , CM000664.2:g.144398807_144398810delinsTAGA	GRCh38
NC_000002.11:g.145156374_145156377delinsTAGA , CM000664.1:g.145156374_145156377delinsTAGA	GRCh37
NC_000002.10:g.144872844_144872847delinsTAGA	NCBI36
NG_016431.1:g.126582_126585delinsTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2226_*2229delinsTCTA	ENSP00000508434.1:n.*2226_*2229delinsTCTA
ENST00000440875.6:c.1600_1603delinsTCTA	ENSP00000475553.3:p.Ser534=
ENST00000627532.3:c.2377_2380delinsTCTA MANE Select	ENSP00000487174.1:p.Ser793=
ENST00000636026.2:c.2377_2380delinsTCTA	ENSP00000490776.1:p.Ser793=
ENST00000636179.1:n.2346_2349delinsTCTA
ENST00000636413.1:c.2041_2044delinsTCTA	ENSP00000490508.1:p.Ser681=
ENST00000636471.1:c.2452_2455delinsTCTA	ENSP00000490317.1:p.Ser818=
ENST00000636732.2:c.*2094_*2097delinsTCTA	ENSP00000490175.1:n.*2094_*2097delinsTCTA
ENST00000636820.1:n.2477_2480delinsTCTA
ENST00000637045.1:c.2041_2044delinsTCTA	ENSP00000490141.1:p.Ser681=
ENST00000637304.1:c.2041_2044delinsTCTA	ENSP00000490872.1:p.Ser681=
ENST00000638007.1:c.2041_2044delinsTCTA	ENSP00000490723.1:p.Ser681=
ENST00000638087.1:c.2041_2044delinsTCTA	ENSP00000490673.1:p.Ser681=
ENST00000638128.1:c.1600_1603delinsTCTA	ENSP00000490934.1:p.Ser534=
ENST00000675069.1:c.-93_-90delinsTCTA	ENSP00000502467.1:n.-93_-90delinsTCTA
ENST00000675145.1:n.2925_2928delinsTCTA
ENST00000303660.8:c.2374_2377delinsTCTA	ENSP00000302501.4:p.Ser792=
ENST00000409487.7:c.2377_2380delinsTCTA	ENSP00000386854.2:p.Ser793=
ENST00000419938.5:c.655+2389_655+2392delinsTCTA	ENSP00000394777.2:n.655+2389_655+2392delinsTCTA
ENST00000440875.5:c.1167+727_1167+730delinsTCTA	ENSP00000475553.2:n.1167+727_1167+730delinsTCTA
ENST00000539609.7:c.2305_2308delinsTCTA	ENSP00000443792.2:p.Ser769=
ENST00000558170.6:c.2377_2380delinsTCTA	ENSP00000454157.1:p.Ser793=
ENST00000627532.2:c.2377_2380delinsTCTA	ENSP00000487174.1:p.Ser793=
NM_001171653.1:c.2305_2308delinsTCTA	NP_001165124.1:p.Ser769=
NM_014795.3:c.2377_2380delinsTCTA	NP_055610.1:p.Ser793=
XM_006712881.2:c.2377_2380delinsTCTA	XP_006712944.1:p.Ser793=
XM_006712882.2:c.2377_2380delinsTCTA	XP_006712945.1:p.Ser793=
XM_011512231.1:c.2368_2371delinsTCTA	XP_011510533.1:p.Ser790=
XM_011512232.1:c.2356_2359delinsTCTA	XP_011510534.1:p.Ser786=
NM_014795.4:c.2377_2380delinsTCTA MANE Select	NP_055610.1:p.Ser793=
NM_001171653.2:c.2305_2308delinsTCTA	NP_001165124.1:p.Ser769=