Canonical Allele Identifier: CA1294881253

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389562_144389563delinsCG , CM000664.2:g.144389562_144389563delinsCG	GRCh38
NC_000002.11:g.145147129_145147130delinsCG , CM000664.1:g.145147129_145147130delinsCG	GRCh37
NC_000002.10:g.144863599_144863600delinsCG	NCBI36
NG_016431.1:g.135829_135830delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3382_*3383delinsCG	ENSP00000508434.1:n.*3382_*3383delinsCG
ENST00000440875.6:c.2756_2757delinsCG	ENSP00000475553.3:p.Thr919=
ENST00000627532.3:c.3533_3534delinsCG MANE Select	ENSP00000487174.1:p.Thr1178=
ENST00000636026.2:c.3421_3422delinsCG	ENSP00000490776.1:p.Arg1141=
ENST00000636179.1:n.3502_3503delinsCG
ENST00000636413.1:c.3197_3198delinsCG	ENSP00000490508.1:p.Thr1066=
ENST00000636471.1:c.3608_3609delinsCG	ENSP00000490317.1:p.Thr1203=
ENST00000636732.2:c.*3250_*3251delinsCG	ENSP00000490175.1:n.*3250_*3251delinsCG
ENST00000636820.1:n.3633_3634delinsCG
ENST00000637045.1:c.3197_3198delinsCG	ENSP00000490141.1:p.Thr1066=
ENST00000637304.1:c.3197_3198delinsCG	ENSP00000490872.1:p.Thr1066=
ENST00000638007.1:c.3197_3198delinsCG	ENSP00000490723.1:p.Thr1066=
ENST00000638087.1:c.3197_3198delinsCG	ENSP00000490673.1:p.Thr1066=
ENST00000638128.1:c.2756_2757delinsCG	ENSP00000490934.1:p.Thr919=
ENST00000639389.1:c.151+6849_151+6850delinsCG	ENSP00000492572.1:n.151+6849_151+6850delinsCG
ENST00000647488.1:c.753_754delinsCG	ENSP00000494820.1:n.753_754delinsCG
ENST00000675069.1:c.1064_1065delinsCG	ENSP00000502467.1:p.Thr355=
ENST00000303660.8:c.3530_3531delinsCG	ENSP00000302501.4:p.Thr1177=
ENST00000409487.7:c.3533_3534delinsCG	ENSP00000386854.2:p.Thr1178=
ENST00000419938.5:c.656-681_656-680delinsCG	ENSP00000394777.2:n.656-681_656-680delinsCG
ENST00000539609.7:c.3461_3462delinsCG	ENSP00000443792.2:p.Thr1154=
ENST00000558170.6:c.3533_3534delinsCG	ENSP00000454157.1:p.Thr1178=
ENST00000627532.2:c.3533_3534delinsCG	ENSP00000487174.1:p.Thr1178=
NM_001171653.1:c.3461_3462delinsCG	NP_001165124.1:p.Thr1154=
NM_014795.3:c.3533_3534delinsCG	NP_055610.1:p.Thr1178=
XM_006712881.2:c.3533_3534delinsCG	XP_006712944.1:p.Thr1178=
XM_006712882.2:c.3533_3534delinsCG	XP_006712945.1:p.Thr1178=
XM_011512231.1:c.3524_3525delinsCG	XP_011510533.1:p.Thr1175=
XM_011512232.1:c.3512_3513delinsCG	XP_011510534.1:p.Thr1171=
NM_014795.4:c.3533_3534delinsCG MANE Select	NP_055610.1:p.Thr1178=
NM_001171653.2:c.3461_3462delinsCG	NP_001165124.1:p.Thr1154=