Canonical Allele Identifier: CA1294885024

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398779_144398783delinsGGAGT , CM000664.2:g.144398779_144398783delinsGGAGT	GRCh38
NC_000002.11:g.145156346_145156350delinsGGAGT , CM000664.1:g.145156346_145156350delinsGGAGT	GRCh37
NC_000002.10:g.144872816_144872820delinsGGAGT	NCBI36
NG_016431.1:g.126609_126613delinsACTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2253_*2257delinsACTCC	ENSP00000508434.1:n.*2253_*2257delinsACTCC
ENST00000440875.6:c.1627_1631delinsACTCC	ENSP00000475553.3:p.Thr543=
ENST00000627532.3:c.2404_2408delinsACTCC MANE Select	ENSP00000487174.1:p.Thr802=
ENST00000636026.2:c.2404_2408delinsACTCC	ENSP00000490776.1:p.Thr802=
ENST00000636179.1:n.2373_2377delinsACTCC
ENST00000636413.1:c.2068_2072delinsACTCC	ENSP00000490508.1:p.Thr690=
ENST00000636471.1:c.2479_2483delinsACTCC	ENSP00000490317.1:p.Thr827=
ENST00000636732.2:c.*2121_*2125delinsACTCC	ENSP00000490175.1:n.*2121_*2125delinsACTCC
ENST00000636820.1:n.2504_2508delinsACTCC
ENST00000637045.1:c.2068_2072delinsACTCC	ENSP00000490141.1:p.Thr690=
ENST00000637304.1:c.2068_2072delinsACTCC	ENSP00000490872.1:p.Thr690=
ENST00000638007.1:c.2068_2072delinsACTCC	ENSP00000490723.1:p.Thr690=
ENST00000638087.1:c.2068_2072delinsACTCC	ENSP00000490673.1:p.Thr690=
ENST00000638128.1:c.1627_1631delinsACTCC	ENSP00000490934.1:p.Thr543=
ENST00000675069.1:c.-66_-62delinsACTCC	ENSP00000502467.1:n.-66_-62delinsACTCC
ENST00000675145.1:n.2952_2956delinsACTCC
ENST00000303660.8:c.2401_2405delinsACTCC	ENSP00000302501.4:p.Thr801=
ENST00000409487.7:c.2404_2408delinsACTCC	ENSP00000386854.2:p.Thr802=
ENST00000419938.5:c.655+2416_655+2420delinsACTCC	ENSP00000394777.2:n.655+2416_655+2420delinsACTCC
ENST00000440875.5:c.1167+754_1167+758delinsACTCC	ENSP00000475553.2:n.1167+754_1167+758delinsACTCC
ENST00000539609.7:c.2332_2336delinsACTCC	ENSP00000443792.2:p.Thr778=
ENST00000558170.6:c.2404_2408delinsACTCC	ENSP00000454157.1:p.Thr802=
ENST00000627532.2:c.2404_2408delinsACTCC	ENSP00000487174.1:p.Thr802=
NM_001171653.1:c.2332_2336delinsACTCC	NP_001165124.1:p.Thr778=
NM_014795.3:c.2404_2408delinsACTCC	NP_055610.1:p.Thr802=
XM_006712881.2:c.2404_2408delinsACTCC	XP_006712944.1:p.Thr802=
XM_006712882.2:c.2404_2408delinsACTCC	XP_006712945.1:p.Thr802=
XM_011512231.1:c.2395_2399delinsACTCC	XP_011510533.1:p.Thr799=
XM_011512232.1:c.2383_2387delinsACTCC	XP_011510534.1:p.Thr795=
NM_014795.4:c.2404_2408delinsACTCC MANE Select	NP_055610.1:p.Thr802=
NM_001171653.2:c.2332_2336delinsACTCC	NP_001165124.1:p.Thr778=