Canonical Allele Identifier: CA10583992
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 242351
ClinVar RCV Id: RCV000234801
dbSNP Id: rs878855329

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398509_144398515del , CM000664.2:g.144398509_144398515del GRCh38
NC_000002.11:g.145156076_145156082del , CM000664.1:g.145156076_145156082del GRCh37
NC_000002.10:g.144872546_144872552del NCBI36
NG_016431.1:g.126877_126883del

Transcript Alleles

HGVS Amino-acid change
ENST00000689298.1:c.*2521_*2527del ENSP00000508434.1:n.*2521_*2527del
ENST00000440875.6:c.1895_1901del ENSP00000475553.3:p.Ala632ValfsTer?
ENST00000627532.3:c.2672_2678del MANE Select ENSP00000487174.1:p.Ala891ValfsTer?
ENST00000636026.2:c.2672_2678del ENSP00000490776.1:p.Ala891ValfsTer?
ENST00000636179.1:n.2641_2647del
ENST00000636413.1:c.2336_2342del ENSP00000490508.1:p.Ala779ValfsTer?
ENST00000636471.1:c.2747_2753del ENSP00000490317.1:p.Ala916ValfsTer?
ENST00000636732.2:c.*2389_*2395del ENSP00000490175.1:n.*2389_*2395del
ENST00000636820.1:n.2772_2778del
ENST00000637045.1:c.2336_2342del ENSP00000490141.1:p.Ala779ValfsTer?
ENST00000637304.1:c.2336_2342del ENSP00000490872.1:p.Ala779ValfsTer?
ENST00000638007.1:c.2336_2342del ENSP00000490723.1:p.Ala779ValfsTer?
ENST00000638087.1:c.2336_2342del ENSP00000490673.1:p.Ala779ValfsTer?
ENST00000638128.1:c.1895_1901del ENSP00000490934.1:p.Ala632ValfsTer?
ENST00000675069.1:c.203_209del ENSP00000502467.1:p.Ala68ValfsTer?
ENST00000303660.8:c.2669_2675del ENSP00000302501.4:p.Ala890ValfsTer?
ENST00000409487.7:c.2672_2678del ENSP00000386854.2:p.Ala891ValfsTer?
ENST00000419938.5:c.655+2684_655+2690del ENSP00000394777.2:n.655+2684_655+2690del
ENST00000440875.5:c.1168-587_1168-581del ENSP00000475553.2:n.1168-587_1168-581del
ENST00000539609.7:c.2600_2606del ENSP00000443792.2:p.Ala867ValfsTer?
ENST00000558170.6:c.2672_2678del ENSP00000454157.1:p.Ala891ValfsTer?
ENST00000627532.2:c.2672_2678del ENSP00000487174.1:p.Ala891ValfsTer?
NM_001171653.1:c.2600_2606del NP_001165124.1:p.Ala867ValfsTer?
NM_014795.3:c.2672_2678del NP_055610.1:p.Ala891ValfsTer?
XM_006712881.2:c.2672_2678del XP_006712944.1:p.Ala891ValfsTer?
XM_006712882.2:c.2672_2678del XP_006712945.1:p.Ala891ValfsTer?
XM_011512231.1:c.2663_2669del XP_011510533.1:p.Ala888ValfsTer?
XM_011512232.1:c.2651_2657del XP_011510534.1:p.Ala884ValfsTer?
NM_014795.4:c.2672_2678del MANE Select NP_055610.1:p.Ala891ValfsTer?
NM_001171653.2:c.2600_2606del NP_001165124.1:p.Ala867ValfsTer?