Canonical Allele Identifier: CA647604966

Gene: ZEB2

Linked Data

• COSMIC: COSN21017571

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389435_144389436insC , CM000664.2:g.144389435_144389436insC	GRCh38
NC_000002.11:g.145147002_145147003insC , CM000664.1:g.145147002_145147003insC	GRCh37
NC_000002.10:g.144863472_144863473insC	NCBI36
NG_016431.1:g.135956_135957insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3509_*3510insG	ENSP00000508434.1:n.*3509_*3510insG
ENST00000440875.6:c.*15_*16insG	ENSP00000475553.3:n.*15_*16insG
ENST00000627532.3:c.*15_*16insG MANE Select	ENSP00000487174.1:n.*15_*16insG
ENST00000636026.2:c.3548_3549insG	ENSP00000490776.1:p.Phe1183LeufsTer2
ENST00000636179.1:n.3629_3630insG
ENST00000636413.1:c.*15_*16insG	ENSP00000490508.1:n.*15_*16insG
ENST00000636471.1:c.*15_*16insG	ENSP00000490317.1:n.*15_*16insG
ENST00000636732.2:c.*3377_*3378insG	ENSP00000490175.1:n.*3377_*3378insG
ENST00000636820.1:n.3760_3761insG
ENST00000637045.1:c.*15_*16insG	ENSP00000490141.1:n.*15_*16insG
ENST00000637304.1:c.*15_*16insG	ENSP00000490872.1:n.*15_*16insG
ENST00000638007.1:c.*15_*16insG	ENSP00000490723.1:n.*15_*16insG
ENST00000638087.1:c.*15_*16insG	ENSP00000490673.1:n.*15_*16insG
ENST00000638128.1:c.*15_*16insG	ENSP00000490934.1:n.*15_*16insG
ENST00000639389.1:c.151+6976_151+6977insG	ENSP00000492572.1:n.151+6976_151+6977insG
ENST00000647488.1:c.880_881insG	ENSP00000494820.1:n.880_881insG
ENST00000675069.1:c.*15_*16insG	ENSP00000502467.1:n.*15_*16insG
ENST00000303660.8:c.*15_*16insG	ENSP00000302501.4:n.*15_*16insG
ENST00000409487.7:c.*15_*16insG	ENSP00000386854.2:n.*15_*16insG
ENST00000419938.5:c.656-554_656-553insG	ENSP00000394777.2:n.656-554_656-553insG
ENST00000539609.7:c.*15_*16insG	ENSP00000443792.2:n.*15_*16insG
ENST00000558170.6:c.*15_*16insG	ENSP00000454157.1:n.*15_*16insG
ENST00000627532.2:c.*15_*16insG	ENSP00000487174.1:n.*15_*16insG
NM_001171653.1:c.*15_*16insG	NP_001165124.1:n.*15_*16insG
NM_014795.3:c.*15_*16insG	NP_055610.1:n.*15_*16insG
XM_006712881.2:c.*15_*16insG	XP_006712944.1:n.*15_*16insG
XM_006712882.2:c.*15_*16insG	XP_006712945.1:n.*15_*16insG
XM_011512231.1:c.*15_*16insG	XP_011510533.1:n.*15_*16insG
XM_011512232.1:c.*15_*16insG	XP_011510534.1:n.*15_*16insG
NM_014795.4:c.*15_*16insG MANE Select	NP_055610.1:n.*15_*16insG
NM_001171653.2:c.*15_*16insG	NP_001165124.1:n.*15_*16insG