Canonical Allele Identifier: CA267213
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95635
dbSNP Id: rs398124280

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389732_144389737delinsCATTA , CM000664.2:g.144389732_144389737delinsCATTA GRCh38
NC_000002.11:g.145147299_145147304delinsCATTA , CM000664.1:g.145147299_145147304delinsCATTA GRCh37
NC_000002.10:g.144863769_144863774delinsCATTA NCBI36
NG_016431.1:g.135655_135660delinsTAATG

Transcript Alleles

HGVS Amino-acid change
ENST00000689298.1:c.*3208_*3213delinsTAATG ENSP00000508434.1:n.*3208_*3213delinsTAAT...
ENST00000440875.6:c.2582_2587delinsTAATG ENSP00000475553.3:p.Gly861ValfsTer?
ENST00000627532.3:c.3359_3364delinsTAATG MANE Select ENSP00000487174.1:p.Gly1120ValfsTer?
ENST00000636026.2:c.3247_3252delinsTAATG ENSP00000490776.1:p.Gly1083Ter
ENST00000636179.1:n.3328_3333delinsTAATG
ENST00000636413.1:c.3023_3028delinsTAATG ENSP00000490508.1:p.Gly1008ValfsTer?
ENST00000636471.1:c.3434_3439delinsTAATG ENSP00000490317.1:p.Gly1145ValfsTer?
ENST00000636732.2:c.*3076_*3081delinsTAATG ENSP00000490175.1:n.*3076_*3081delinsTAAT...
ENST00000636820.1:n.3459_3464delinsTAATG
ENST00000637045.1:c.3023_3028delinsTAATG ENSP00000490141.1:p.Gly1008ValfsTer?
ENST00000637304.1:c.3023_3028delinsTAATG ENSP00000490872.1:p.Gly1008ValfsTer?
ENST00000638007.1:c.3023_3028delinsTAATG ENSP00000490723.1:p.Gly1008ValfsTer?
ENST00000638087.1:c.3023_3028delinsTAATG ENSP00000490673.1:p.Gly1008ValfsTer?
ENST00000638128.1:c.2582_2587delinsTAATG ENSP00000490934.1:p.Gly861ValfsTer?
ENST00000639389.1:c.151+6675_151+6680delinsTAATG ENSP00000492572.1:n.151+6675_151+6680deli...
ENST00000647488.1:c.579_584delinsTAATG ENSP00000494820.1:n.579_584delinsTAATG
ENST00000675069.1:c.890_895delinsTAATG ENSP00000502467.1:p.Gly297ValfsTer?
ENST00000303660.8:c.3356_3361delinsTAATG ENSP00000302501.4:p.Gly1119ValfsTer?
ENST00000409487.7:c.3359_3364delinsTAATG ENSP00000386854.2:p.Gly1120ValfsTer?
ENST00000419938.5:c.656-855_656-850delinsTAATG ENSP00000394777.2:n.656-855_656-850delins...
ENST00000539609.7:c.3287_3292delinsTAATG ENSP00000443792.2:p.Gly1096ValfsTer?
ENST00000558170.6:c.3359_3364delinsTAATG ENSP00000454157.1:p.Gly1120ValfsTer?
ENST00000627532.2:c.3359_3364delinsTAATG ENSP00000487174.1:p.Gly1120ValfsTer?
NM_001171653.1:c.3287_3292delinsTAATG NP_001165124.1:p.Gly1096ValfsTer?
NM_014795.3:c.3359_3364delinsTAATG NP_055610.1:p.Gly1120ValfsTer?
XM_006712881.2:c.3359_3364delinsTAATG XP_006712944.1:p.Gly1120ValfsTer?
XM_006712882.2:c.3359_3364delinsTAATG XP_006712945.1:p.Gly1120ValfsTer?
XM_011512231.1:c.3350_3355delinsTAATG XP_011510533.1:p.Gly1117ValfsTer?
XM_011512232.1:c.3338_3343delinsTAATG XP_011510534.1:p.Gly1113ValfsTer?
NM_014795.4:c.3359_3364delinsTAATG MANE Select NP_055610.1:p.Gly1120ValfsTer?
NM_001171653.2:c.3287_3292delinsTAATG NP_001165124.1:p.Gly1096ValfsTer?