Canonical Allele Identifier: CA1294881263

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389596_144389597delinsCT , CM000664.2:g.144389596_144389597delinsCT	GRCh38
NC_000002.11:g.145147163_145147164delinsCT , CM000664.1:g.145147163_145147164delinsCT	GRCh37
NC_000002.10:g.144863633_144863634delinsCT	NCBI36
NG_016431.1:g.135795_135796delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3348_*3349delinsAG	ENSP00000508434.1:n.*3348_*3349delinsAG
ENST00000440875.6:c.2722_2723delinsAG	ENSP00000475553.3:p.Ser908=
ENST00000627532.3:c.3499_3500delinsAG MANE Select	ENSP00000487174.1:p.Ser1167=
ENST00000636026.2:c.3387_3388delinsAG	ENSP00000490776.1:p.Lys1129=
ENST00000636179.1:n.3468_3469delinsAG
ENST00000636413.1:c.3163_3164delinsAG	ENSP00000490508.1:p.Ser1055=
ENST00000636471.1:c.3574_3575delinsAG	ENSP00000490317.1:p.Ser1192=
ENST00000636732.2:c.*3216_*3217delinsAG	ENSP00000490175.1:n.*3216_*3217delinsAG
ENST00000636820.1:n.3599_3600delinsAG
ENST00000637045.1:c.3163_3164delinsAG	ENSP00000490141.1:p.Ser1055=
ENST00000637304.1:c.3163_3164delinsAG	ENSP00000490872.1:p.Ser1055=
ENST00000638007.1:c.3163_3164delinsAG	ENSP00000490723.1:p.Ser1055=
ENST00000638087.1:c.3163_3164delinsAG	ENSP00000490673.1:p.Ser1055=
ENST00000638128.1:c.2722_2723delinsAG	ENSP00000490934.1:p.Ser908=
ENST00000639389.1:c.151+6815_151+6816delinsAG	ENSP00000492572.1:n.151+6815_151+6816delinsAG
ENST00000647488.1:c.719_720delinsAG	ENSP00000494820.1:n.719_720delinsAG
ENST00000675069.1:c.1030_1031delinsAG	ENSP00000502467.1:p.Ser344=
ENST00000303660.8:c.3496_3497delinsAG	ENSP00000302501.4:p.Ser1166=
ENST00000409487.7:c.3499_3500delinsAG	ENSP00000386854.2:p.Ser1167=
ENST00000419938.5:c.656-715_656-714delinsAG	ENSP00000394777.2:n.656-715_656-714delinsAG
ENST00000539609.7:c.3427_3428delinsAG	ENSP00000443792.2:p.Ser1143=
ENST00000558170.6:c.3499_3500delinsAG	ENSP00000454157.1:p.Ser1167=
ENST00000627532.2:c.3499_3500delinsAG	ENSP00000487174.1:p.Ser1167=
NM_001171653.1:c.3427_3428delinsAG	NP_001165124.1:p.Ser1143=
NM_014795.3:c.3499_3500delinsAG	NP_055610.1:p.Ser1167=
XM_006712881.2:c.3499_3500delinsAG	XP_006712944.1:p.Ser1167=
XM_006712882.2:c.3499_3500delinsAG	XP_006712945.1:p.Ser1167=
XM_011512231.1:c.3490_3491delinsAG	XP_011510533.1:p.Ser1164=
XM_011512232.1:c.3478_3479delinsAG	XP_011510534.1:p.Ser1160=
NM_014795.4:c.3499_3500delinsAG MANE Select	NP_055610.1:p.Ser1167=
NM_001171653.2:c.3427_3428delinsAG	NP_001165124.1:p.Ser1143=