Canonical Allele Identifier: CA235591

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 187814
• ClinVar RCV Id: RCV000167555
• dbSNP Id: rs786203992
• MyVariant Identifiers: chr2:g.145156389del (hg19) ; chr2:g.144398822del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398824del , CM000664.2:g.144398824del	GRCh38
NC_000002.11:g.145156391del , CM000664.1:g.145156391del	GRCh37
NC_000002.10:g.144872861del	NCBI36
NG_016431.1:g.126570del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2214del	ENSP00000508434.1:n.*2214del
ENST00000440875.6:c.1588del	ENSP00000475553.3:p.Ser530ProfsTer28
ENST00000627532.3:c.2365del MANE Select	ENSP00000487174.1:p.Ser789ProfsTer28
ENST00000636026.2:c.2365del	ENSP00000490776.1:p.Ser789ProfsTer28
ENST00000636179.1:n.2334del
ENST00000636413.1:c.2029del	ENSP00000490508.1:p.Ser677ProfsTer28
ENST00000636471.1:c.2440del	ENSP00000490317.1:p.Ser814ProfsTer28
ENST00000636732.2:c.*2082del	ENSP00000490175.1:n.*2082del
ENST00000636820.1:n.2465del
ENST00000637045.1:c.2029del	ENSP00000490141.1:p.Ser677ProfsTer28
ENST00000637304.1:c.2029del	ENSP00000490872.1:p.Ser677ProfsTer28
ENST00000638007.1:c.2029del	ENSP00000490723.1:p.Ser677ProfsTer28
ENST00000638087.1:c.2029del	ENSP00000490673.1:p.Ser677ProfsTer28
ENST00000638128.1:c.1588del	ENSP00000490934.1:p.Ser530ProfsTer28
ENST00000675069.1:c.-105del	ENSP00000502467.1:n.-105del
ENST00000675145.1:n.2913del
ENST00000303660.8:c.2362del	ENSP00000302501.4:p.Ser788ProfsTer28
ENST00000409487.7:c.2365del	ENSP00000386854.2:p.Ser789ProfsTer28
ENST00000419938.5:c.655+2377del	ENSP00000394777.2:n.655+2377del
ENST00000440875.5:c.1167+715del	ENSP00000475553.2:n.1167+715del
ENST00000539609.7:c.2293del	ENSP00000443792.2:p.Ser765ProfsTer28
ENST00000558170.6:c.2365del	ENSP00000454157.1:p.Ser789ProfsTer28
ENST00000627532.2:c.2365del	ENSP00000487174.1:p.Ser789ProfsTer28
NM_001171653.1:c.2293del	NP_001165124.1:p.Ser765ProfsTer28
NM_014795.3:c.2365del	NP_055610.1:p.Ser789ProfsTer28
XM_006712881.2:c.2365del	XP_006712944.1:p.Ser789ProfsTer28
XM_006712882.2:c.2365del	XP_006712945.1:p.Ser789ProfsTer28
XM_011512231.1:c.2356del	XP_011510533.1:p.Ser786ProfsTer28
XM_011512232.1:c.2344del	XP_011510534.1:p.Ser782ProfsTer28
NM_014795.4:c.2365del MANE Select	NP_055610.1:p.Ser789ProfsTer28
NM_001171653.2:c.2293del	NP_001165124.1:p.Ser765ProfsTer28