Canonical Allele Identifier: CA1294884078

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396475_144396483delinsCACATGCAT , CM000664.2:g.144396475_144396483delinsCACATGCAT	GRCh38
NC_000002.11:g.145154042_145154050delinsCACATGCAT , CM000664.1:g.145154042_145154050delinsCACATGCAT	GRCh37
NC_000002.10:g.144870512_144870520delinsCACATGCAT	NCBI36
NG_016431.1:g.128909_128917delinsATGCATGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2845_*2853delinsATGCATGTG	ENSP00000508434.1:n.*2845_*2853delinsATGC...
ENST00000440875.6:c.2219_2227delinsATGCATGTG	ENSP00000475553.3:p.Tyr740=
ENST00000627532.3:c.2996_3004delinsATGCATGTG MANE Select	ENSP00000487174.1:p.Tyr999=
ENST00000636026.2:c.2996_3004delinsATGCATGTG	ENSP00000490776.1:p.Tyr999=
ENST00000636179.1:n.2965_2973delinsATGCATGTG
ENST00000636413.1:c.2660_2668delinsATGCATGTG	ENSP00000490508.1:p.Tyr887=
ENST00000636471.1:c.3071_3079delinsATGCATGTG	ENSP00000490317.1:p.Tyr1024=
ENST00000636732.2:c.*2713_*2721delinsATGCATGTG	ENSP00000490175.1:n.*2713_*2721delinsATGC...
ENST00000636820.1:n.3096_3104delinsATGCATGTG
ENST00000637045.1:c.2660_2668delinsATGCATGTG	ENSP00000490141.1:p.Tyr887=
ENST00000637304.1:c.2660_2668delinsATGCATGTG	ENSP00000490872.1:p.Tyr887=
ENST00000638007.1:c.2660_2668delinsATGCATGTG	ENSP00000490723.1:p.Tyr887=
ENST00000638087.1:c.2660_2668delinsATGCATGTG	ENSP00000490673.1:p.Tyr887=
ENST00000638128.1:c.2219_2227delinsATGCATGTG	ENSP00000490934.1:p.Tyr740=
ENST00000639389.1:c.80_88delinsATGCATGTG	ENSP00000492572.1:p.Tyr27=
ENST00000647488.1:c.128_136delinsATGCATGTG	ENSP00000494820.1:p.Tyr43=
ENST00000675069.1:c.527_535delinsATGCATGTG	ENSP00000502467.1:p.Tyr176=
ENST00000303660.8:c.2993_3001delinsATGCATGTG	ENSP00000302501.4:p.Tyr998=
ENST00000409487.7:c.2996_3004delinsATGCATGTG	ENSP00000386854.2:p.Tyr999=
ENST00000419938.5:c.655+4716_655+4724delinsATGCATGTG	ENSP00000394777.2:n.655+4716_655+4724deli...
ENST00000539609.7:c.2924_2932delinsATGCATGTG	ENSP00000443792.2:p.Tyr975=
ENST00000558170.6:c.2996_3004delinsATGCATGTG	ENSP00000454157.1:p.Tyr999=
ENST00000627532.2:c.2996_3004delinsATGCATGTG	ENSP00000487174.1:p.Tyr999=
NM_001171653.1:c.2924_2932delinsATGCATGTG	NP_001165124.1:p.Tyr975=
NM_014795.3:c.2996_3004delinsATGCATGTG	NP_055610.1:p.Tyr999=
XM_006712881.2:c.2996_3004delinsATGCATGTG	XP_006712944.1:p.Tyr999=
XM_006712882.2:c.2996_3004delinsATGCATGTG	XP_006712945.1:p.Tyr999=
XM_011512231.1:c.2987_2995delinsATGCATGTG	XP_011510533.1:p.Tyr996=
XM_011512232.1:c.2975_2983delinsATGCATGTG	XP_011510534.1:p.Tyr992=
NM_014795.4:c.2996_3004delinsATGCATGTG MANE Select	NP_055610.1:p.Tyr999=
NM_001171653.2:c.2924_2932delinsATGCATGTG	NP_001165124.1:p.Tyr975=