Canonical Allele Identifier: CA1294881409

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389997_144389998delinsCT , CM000664.2:g.144389997_144389998delinsCT	GRCh38
NC_000002.11:g.145147564_145147565delinsCT , CM000664.1:g.145147564_145147565delinsCT	GRCh37
NC_000002.10:g.144864034_144864035delinsCT	NCBI36
NG_016431.1:g.135394_135395delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2947_*2948delinsAG	ENSP00000508434.1:n.*2947_*2948delinsAG
ENST00000440875.6:c.2321_2322delinsAG	ENSP00000475553.3:p.Lys774=
ENST00000627532.3:c.3098_3099delinsAG MANE Select	ENSP00000487174.1:p.Lys1033=
ENST00000636026.2:c.3098_3099delinsAG	ENSP00000490776.1:p.Lys1033=
ENST00000636179.1:n.3067_3068delinsAG
ENST00000636413.1:c.2762_2763delinsAG	ENSP00000490508.1:p.Lys921=
ENST00000636471.1:c.3173_3174delinsAG	ENSP00000490317.1:p.Lys1058=
ENST00000636732.2:c.*2815_*2816delinsAG	ENSP00000490175.1:n.*2815_*2816delinsAG
ENST00000636820.1:n.3198_3199delinsAG
ENST00000637045.1:c.2762_2763delinsAG	ENSP00000490141.1:p.Lys921=
ENST00000637304.1:c.2762_2763delinsAG	ENSP00000490872.1:p.Lys921=
ENST00000638007.1:c.2762_2763delinsAG	ENSP00000490723.1:p.Lys921=
ENST00000638087.1:c.2762_2763delinsAG	ENSP00000490673.1:p.Lys921=
ENST00000638128.1:c.2321_2322delinsAG	ENSP00000490934.1:p.Lys774=
ENST00000639389.1:c.151+6414_151+6415delinsAG	ENSP00000492572.1:n.151+6414_151+6415delinsAG
ENST00000647488.1:c.318_319delinsAG	ENSP00000494820.1:n.318_319delinsAG
ENST00000675069.1:c.629_630delinsAG	ENSP00000502467.1:p.Lys210=
ENST00000303660.8:c.3095_3096delinsAG	ENSP00000302501.4:p.Lys1032=
ENST00000409487.7:c.3098_3099delinsAG	ENSP00000386854.2:p.Lys1033=
ENST00000419938.5:c.656-1116_656-1115delinsAG	ENSP00000394777.2:n.656-1116_656-1115delinsAG
ENST00000539609.7:c.3026_3027delinsAG	ENSP00000443792.2:p.Lys1009=
ENST00000558170.6:c.3098_3099delinsAG	ENSP00000454157.1:p.Lys1033=
ENST00000627532.2:c.3098_3099delinsAG	ENSP00000487174.1:p.Lys1033=
NM_001171653.1:c.3026_3027delinsAG	NP_001165124.1:p.Lys1009=
NM_014795.3:c.3098_3099delinsAG	NP_055610.1:p.Lys1033=
XM_006712881.2:c.3098_3099delinsAG	XP_006712944.1:p.Lys1033=
XM_006712882.2:c.3098_3099delinsAG	XP_006712945.1:p.Lys1033=
XM_011512231.1:c.3089_3090delinsAG	XP_011510533.1:p.Lys1030=
XM_011512232.1:c.3077_3078delinsAG	XP_011510534.1:p.Lys1026=
NM_014795.4:c.3098_3099delinsAG MANE Select	NP_055610.1:p.Lys1033=
NM_001171653.2:c.3026_3027delinsAG	NP_001165124.1:p.Lys1009=