Canonical Allele Identifier: CA1294881303

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389695_144389705delinsCCATCCCTCGG , CM000664.2:g.144389695_144389705delinsCCATCCCTCGG	GRCh38
NC_000002.11:g.145147262_145147272delinsCCATCCCTCGG , CM000664.1:g.145147262_145147272delinsCCATCCCTCGG	GRCh37
NC_000002.10:g.144863732_144863742delinsCCATCCCTCGG	NCBI36
NG_016431.1:g.135687_135697delinsCCGAGGGATGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3240_*3250delinsCCGAGGGATGG	ENSP00000508434.1:n.*3240_*3250delinsCCGAGGGATGG
ENST00000440875.6:c.2614_2624delinsCCGAGGGATGG	ENSP00000475553.3:p.Pro872=
ENST00000627532.3:c.3391_3401delinsCCGAGGGATGG MANE Select	ENSP00000487174.1:p.Pro1131=
ENST00000636026.2:c.3279_3289delinsCCGAGGGATGG	ENSP00000490776.1:p.Cys1093=
ENST00000636179.1:n.3360_3370delinsCCGAGGGATGG
ENST00000636413.1:c.3055_3065delinsCCGAGGGATGG	ENSP00000490508.1:p.Pro1019=
ENST00000636471.1:c.3466_3476delinsCCGAGGGATGG	ENSP00000490317.1:p.Pro1156=
ENST00000636732.2:c.*3108_*3118delinsCCGAGGGATGG	ENSP00000490175.1:n.*3108_*3118delinsCCGAGGGATGG
ENST00000636820.1:n.3491_3501delinsCCGAGGGATGG
ENST00000637045.1:c.3055_3065delinsCCGAGGGATGG	ENSP00000490141.1:p.Pro1019=
ENST00000637304.1:c.3055_3065delinsCCGAGGGATGG	ENSP00000490872.1:p.Pro1019=
ENST00000638007.1:c.3055_3065delinsCCGAGGGATGG	ENSP00000490723.1:p.Pro1019=
ENST00000638087.1:c.3055_3065delinsCCGAGGGATGG	ENSP00000490673.1:p.Pro1019=
ENST00000638128.1:c.2614_2624delinsCCGAGGGATGG	ENSP00000490934.1:p.Pro872=
ENST00000639389.1:c.151+6707_151+6717delinsCCGAGGGATGG	ENSP00000492572.1:n.151+6707_151+6717delinsCCGAGGGATGG
ENST00000647488.1:c.611_621delinsCCGAGGGATGG	ENSP00000494820.1:n.611_621delinsCCGAGGGATGG
ENST00000675069.1:c.922_932delinsCCGAGGGATGG	ENSP00000502467.1:p.Pro308=
ENST00000303660.8:c.3388_3398delinsCCGAGGGATGG	ENSP00000302501.4:p.Pro1130=
ENST00000409487.7:c.3391_3401delinsCCGAGGGATGG	ENSP00000386854.2:p.Pro1131=
ENST00000419938.5:c.656-823_656-813delinsCCGAGGGATGG	ENSP00000394777.2:n.656-823_656-813delinsCCGAGGGATGG
ENST00000539609.7:c.3319_3329delinsCCGAGGGATGG	ENSP00000443792.2:p.Pro1107=
ENST00000558170.6:c.3391_3401delinsCCGAGGGATGG	ENSP00000454157.1:p.Pro1131=
ENST00000627532.2:c.3391_3401delinsCCGAGGGATGG	ENSP00000487174.1:p.Pro1131=
NM_001171653.1:c.3319_3329delinsCCGAGGGATGG	NP_001165124.1:p.Pro1107=
NM_014795.3:c.3391_3401delinsCCGAGGGATGG	NP_055610.1:p.Pro1131=
XM_006712881.2:c.3391_3401delinsCCGAGGGATGG	XP_006712944.1:p.Pro1131=
XM_006712882.2:c.3391_3401delinsCCGAGGGATGG	XP_006712945.1:p.Pro1131=
XM_011512231.1:c.3382_3392delinsCCGAGGGATGG	XP_011510533.1:p.Pro1128=
XM_011512232.1:c.3370_3380delinsCCGAGGGATGG	XP_011510534.1:p.Pro1124=
NM_014795.4:c.3391_3401delinsCCGAGGGATGG MANE Select	NP_055610.1:p.Pro1131=
NM_001171653.2:c.3319_3329delinsCCGAGGGATGG	NP_001165124.1:p.Pro1107=