Canonical Allele Identifier: CA1294884083

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396491_144396493delinsACT , CM000664.2:g.144396491_144396493delinsACT	GRCh38
NC_000002.11:g.145154058_145154060delinsACT , CM000664.1:g.145154058_145154060delinsACT	GRCh37
NC_000002.10:g.144870528_144870530delinsACT	NCBI36
NG_016431.1:g.128899_128901delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2835_*2837delinsAGT	ENSP00000508434.1:n.*2835_*2837delinsAGT
ENST00000440875.6:c.2209_2211delinsAGT	ENSP00000475553.3:p.Ser737=
ENST00000627532.3:c.2986_2988delinsAGT MANE Select	ENSP00000487174.1:p.Ser996=
ENST00000636026.2:c.2986_2988delinsAGT	ENSP00000490776.1:p.Ser996=
ENST00000636179.1:n.2955_2957delinsAGT
ENST00000636413.1:c.2650_2652delinsAGT	ENSP00000490508.1:p.Ser884=
ENST00000636471.1:c.3061_3063delinsAGT	ENSP00000490317.1:p.Ser1021=
ENST00000636732.2:c.*2703_*2705delinsAGT	ENSP00000490175.1:n.*2703_*2705delinsAGT
ENST00000636820.1:n.3086_3088delinsAGT
ENST00000637045.1:c.2650_2652delinsAGT	ENSP00000490141.1:p.Ser884=
ENST00000637304.1:c.2650_2652delinsAGT	ENSP00000490872.1:p.Ser884=
ENST00000638007.1:c.2650_2652delinsAGT	ENSP00000490723.1:p.Ser884=
ENST00000638087.1:c.2650_2652delinsAGT	ENSP00000490673.1:p.Ser884=
ENST00000638128.1:c.2209_2211delinsAGT	ENSP00000490934.1:p.Ser737=
ENST00000639389.1:c.70_72delinsAGT	ENSP00000492572.1:p.Ser24=
ENST00000647488.1:c.118_120delinsAGT	ENSP00000494820.1:p.Ser40=
ENST00000675069.1:c.517_519delinsAGT	ENSP00000502467.1:p.Ser173=
ENST00000303660.8:c.2983_2985delinsAGT	ENSP00000302501.4:p.Ser995=
ENST00000409487.7:c.2986_2988delinsAGT	ENSP00000386854.2:p.Ser996=
ENST00000419938.5:c.655+4706_655+4708delinsAGT	ENSP00000394777.2:n.655+4706_655+4708delinsAGT
ENST00000539609.7:c.2914_2916delinsAGT	ENSP00000443792.2:p.Ser972=
ENST00000558170.6:c.2986_2988delinsAGT	ENSP00000454157.1:p.Ser996=
ENST00000627532.2:c.2986_2988delinsAGT	ENSP00000487174.1:p.Ser996=
NM_001171653.1:c.2914_2916delinsAGT	NP_001165124.1:p.Ser972=
NM_014795.3:c.2986_2988delinsAGT	NP_055610.1:p.Ser996=
XM_006712881.2:c.2986_2988delinsAGT	XP_006712944.1:p.Ser996=
XM_006712882.2:c.2986_2988delinsAGT	XP_006712945.1:p.Ser996=
XM_011512231.1:c.2977_2979delinsAGT	XP_011510533.1:p.Ser993=
XM_011512232.1:c.2965_2967delinsAGT	XP_011510534.1:p.Ser989=
NM_014795.4:c.2986_2988delinsAGT MANE Select	NP_055610.1:p.Ser996=
NM_001171653.2:c.2914_2916delinsAGT	NP_001165124.1:p.Ser972=