Canonical Allele Identifier: CA2661333312

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144398770-A-AAGCTGTTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398771_144398779dup , CM000664.2:g.144398771_144398779dup	GRCh38
NC_000002.11:g.145156338_145156346dup , CM000664.1:g.145156338_145156346dup	GRCh37
NC_000002.10:g.144872808_144872816dup	NCBI36
NG_016431.1:g.126613_126621dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2257_*2265dup	ENSP00000508434.1:n.*2257_*2265dup
ENST00000440875.6:c.1631_1639dup	ENSP00000475553.3:p.Ser546_Phe547insSerAsnSer
ENST00000627532.3:c.2408_2416dup MANE Select	ENSP00000487174.1:p.Ser805_Phe806insSerAsnSer
ENST00000636026.2:c.2408_2416dup	ENSP00000490776.1:p.Ser805_Phe806insSerAsnSer
ENST00000636179.1:n.2377_2385dup
ENST00000636413.1:c.2072_2080dup	ENSP00000490508.1:p.Ser693_Phe694insSerAsnSer
ENST00000636471.1:c.2483_2491dup	ENSP00000490317.1:p.Ser830_Phe831insSerAsnSer
ENST00000636732.2:c.*2125_*2133dup	ENSP00000490175.1:n.*2125_*2133dup
ENST00000636820.1:n.2508_2516dup
ENST00000637045.1:c.2072_2080dup	ENSP00000490141.1:p.Ser693_Phe694insSerAsnSer
ENST00000637304.1:c.2072_2080dup	ENSP00000490872.1:p.Ser693_Phe694insSerAsnSer
ENST00000638007.1:c.2072_2080dup	ENSP00000490723.1:p.Ser693_Phe694insSerAsnSer
ENST00000638087.1:c.2072_2080dup	ENSP00000490673.1:p.Ser693_Phe694insSerAsnSer
ENST00000638128.1:c.1631_1639dup	ENSP00000490934.1:p.Ser546_Phe547insSerAsnSer
ENST00000675069.1:c.-62_-54dup	ENSP00000502467.1:n.-62_-54dup
ENST00000675145.1:n.2956_2964dup
ENST00000303660.8:c.2405_2413dup	ENSP00000302501.4:p.Ser804_Phe805insSerAsnSer
ENST00000409487.7:c.2408_2416dup	ENSP00000386854.2:p.Ser805_Phe806insSerAsnSer
ENST00000419938.5:c.655+2420_655+2428dup	ENSP00000394777.2:n.655+2420_655+2428dup
ENST00000440875.5:c.1167+758_1167+766dup	ENSP00000475553.2:n.1167+758_1167+766dup
ENST00000539609.7:c.2336_2344dup	ENSP00000443792.2:p.Ser781_Phe782insSerAsnSer
ENST00000558170.6:c.2408_2416dup	ENSP00000454157.1:p.Ser805_Phe806insSerAsnSer
ENST00000627532.2:c.2408_2416dup	ENSP00000487174.1:p.Ser805_Phe806insSerAsnSer
NM_001171653.1:c.2336_2344dup	NP_001165124.1:p.Ser781_Phe782insSerAsnSer
NM_014795.3:c.2408_2416dup	NP_055610.1:p.Ser805_Phe806insSerAsnSer
XM_006712881.2:c.2408_2416dup	XP_006712944.1:p.Ser805_Phe806insSerAsnSer
XM_006712882.2:c.2408_2416dup	XP_006712945.1:p.Ser805_Phe806insSerAsnSer
XM_011512231.1:c.2399_2407dup	XP_011510533.1:p.Ser802_Phe803insSerAsnSer
XM_011512232.1:c.2387_2395dup	XP_011510534.1:p.Ser798_Phe799insSerAsnSer
NM_014795.4:c.2408_2416dup MANE Select	NP_055610.1:p.Ser805_Phe806insSerAsnSer
NM_001171653.2:c.2336_2344dup	NP_001165124.1:p.Ser781_Phe782insSerAsnSer