Canonical Allele Identifier: CA1898252

Gene: ZEB2

Linked Data

• dbSNP Id: rs778676709
• ExAC: 2:145156374 TAGA / T
• gnomAD v2: 2-145156374-TAGA-T
• gnomAD v4: 2-144398807-TAGA-T
• MyVariant Identifiers: chr2:g.145156375_145156377del (hg19) ; chr2:g.144398808_144398810del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398811_144398813del , CM000664.2:g.144398811_144398813del	GRCh38
NC_000002.11:g.145156378_145156380del , CM000664.1:g.145156378_145156380del	GRCh37
NC_000002.10:g.144872848_144872850del	NCBI36
NG_016431.1:g.126582_126584del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2226_*2228del	ENSP00000508434.1:n.*2226_*2228del
ENST00000440875.6:c.1600_1602del	ENSP00000475553.3:p.Ser534del
ENST00000627532.3:c.2377_2379del MANE Select	ENSP00000487174.1:p.Ser793del
ENST00000636026.2:c.2377_2379del	ENSP00000490776.1:p.Ser793del
ENST00000636179.1:n.2346_2348del
ENST00000636413.1:c.2041_2043del	ENSP00000490508.1:p.Ser681del
ENST00000636471.1:c.2452_2454del	ENSP00000490317.1:p.Ser818del
ENST00000636732.2:c.*2094_*2096del	ENSP00000490175.1:n.*2094_*2096del
ENST00000636820.1:n.2477_2479del
ENST00000637045.1:c.2041_2043del	ENSP00000490141.1:p.Ser681del
ENST00000637304.1:c.2041_2043del	ENSP00000490872.1:p.Ser681del
ENST00000638007.1:c.2041_2043del	ENSP00000490723.1:p.Ser681del
ENST00000638087.1:c.2041_2043del	ENSP00000490673.1:p.Ser681del
ENST00000638128.1:c.1600_1602del	ENSP00000490934.1:p.Ser534del
ENST00000675069.1:c.-93_-91del	ENSP00000502467.1:n.-93_-91del
ENST00000675145.1:n.2925_2927del
ENST00000303660.8:c.2374_2376del	ENSP00000302501.4:p.Ser792del
ENST00000409487.7:c.2377_2379del	ENSP00000386854.2:p.Ser793del
ENST00000419938.5:c.655+2389_655+2391del	ENSP00000394777.2:n.655+2389_655+2391del
ENST00000440875.5:c.1167+727_1167+729del	ENSP00000475553.2:n.1167+727_1167+729del
ENST00000539609.7:c.2305_2307del	ENSP00000443792.2:p.Ser769del
ENST00000558170.6:c.2377_2379del	ENSP00000454157.1:p.Ser793del
ENST00000627532.2:c.2377_2379del	ENSP00000487174.1:p.Ser793del
NM_001171653.1:c.2305_2307del	NP_001165124.1:p.Ser769del
NM_014795.3:c.2377_2379del	NP_055610.1:p.Ser793del
XM_006712881.2:c.2377_2379del	XP_006712944.1:p.Ser793del
XM_006712882.2:c.2377_2379del	XP_006712945.1:p.Ser793del
XM_011512231.1:c.2368_2370del	XP_011510533.1:p.Ser790del
XM_011512232.1:c.2356_2358del	XP_011510534.1:p.Ser786del
NM_014795.4:c.2377_2379del MANE Select	NP_055610.1:p.Ser793del
NM_001171653.2:c.2305_2307del	NP_001165124.1:p.Ser769del