Canonical Allele Identifier: CA348708238
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398728A>T , CM000664.2:g.144398728A>T GRCh38
NC_000002.11:g.145156295A>T , CM000664.1:g.145156295A>T GRCh37
NC_000002.10:g.144872765A>T NCBI36
NG_016431.1:g.126664T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2308T>A ENSP00000508434.1:n.*2308T>A
ENST00000440875.6:c.1682T>A ENSP00000475553.3:p.Leu561Ter
ENST00000627532.3:c.2459T>A MANE Select ENSP00000487174.1:p.Leu820Ter
ENST00000636026.2:c.2459T>A ENSP00000490776.1:p.Leu820Ter
ENST00000636179.1:n.2428T>A
ENST00000636413.1:c.2123T>A ENSP00000490508.1:p.Leu708Ter
ENST00000636471.1:c.2534T>A ENSP00000490317.1:p.Leu845Ter
ENST00000636732.2:c.*2176T>A ENSP00000490175.1:n.*2176T>A
ENST00000636820.1:n.2559T>A
ENST00000637045.1:c.2123T>A ENSP00000490141.1:p.Leu708Ter
ENST00000637304.1:c.2123T>A ENSP00000490872.1:p.Leu708Ter
ENST00000638007.1:c.2123T>A ENSP00000490723.1:p.Leu708Ter
ENST00000638087.1:c.2123T>A ENSP00000490673.1:p.Leu708Ter
ENST00000638128.1:c.1682T>A ENSP00000490934.1:p.Leu561Ter
ENST00000675069.1:c.-11T>A ENSP00000502467.1:n.-11T>A
ENST00000675145.1:n.3007T>A
ENST00000303660.8:c.2456T>A ENSP00000302501.4:p.Leu819Ter
ENST00000409487.7:c.2459T>A ENSP00000386854.2:p.Leu820Ter
ENST00000419938.5:c.655+2471T>A ENSP00000394777.2:n.655+2471T>A
ENST00000440875.5:c.1168-800T>A ENSP00000475553.2:n.1168-800T>A
ENST00000539609.7:c.2387T>A ENSP00000443792.2:p.Leu796Ter
ENST00000558170.6:c.2459T>A ENSP00000454157.1:p.Leu820Ter
ENST00000627532.2:c.2459T>A ENSP00000487174.1:p.Leu820Ter
NM_001171653.1:c.2387T>A NP_001165124.1:p.Leu796Ter
NM_014795.3:c.2459T>A NP_055610.1:p.Leu820Ter
XM_006712881.2:c.2459T>A XP_006712944.1:p.Leu820Ter
XM_006712882.2:c.2459T>A XP_006712945.1:p.Leu820Ter
XM_011512231.1:c.2450T>A XP_011510533.1:p.Leu817Ter
XM_011512232.1:c.2438T>A XP_011510534.1:p.Leu813Ter
NM_014795.4:c.2459T>A MANE Select NP_055610.1:p.Leu820Ter
NM_001171653.2:c.2387T>A NP_001165124.1:p.Leu796Ter