Canonical Allele Identifier: CA2586969980

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389761_144389764del , CM000664.2:g.144389761_144389764del	GRCh38
NC_000002.11:g.145147328_145147331del , CM000664.1:g.145147328_145147331del	GRCh37
NC_000002.10:g.144863798_144863801del	NCBI36
NG_016431.1:g.135631_135634del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3184_*3187del	ENSP00000508434.1:n.*3184_*3187del
ENST00000440875.6:c.2558_2561del	ENSP00000475553.3:p.Tyr853CysfsTer?
ENST00000627532.3:c.3335_3338del MANE Select	ENSP00000487174.1:p.Tyr1112CysfsTer?
ENST00000636026.2:c.3231-8_3231-5del	ENSP00000490776.1:n.3231-8_3231-5del
ENST00000636179.1:n.3304_3307del
ENST00000636413.1:c.2999_3002del	ENSP00000490508.1:p.Tyr1000CysfsTer?
ENST00000636471.1:c.3410_3413del	ENSP00000490317.1:p.Tyr1137CysfsTer?
ENST00000636732.2:c.*3052_*3055del	ENSP00000490175.1:n.*3052_*3055del
ENST00000636820.1:n.3435_3438del
ENST00000637045.1:c.2999_3002del	ENSP00000490141.1:p.Tyr1000CysfsTer?
ENST00000637304.1:c.2999_3002del	ENSP00000490872.1:p.Tyr1000CysfsTer?
ENST00000638007.1:c.2999_3002del	ENSP00000490723.1:p.Tyr1000CysfsTer?
ENST00000638087.1:c.2999_3002del	ENSP00000490673.1:p.Tyr1000CysfsTer?
ENST00000638128.1:c.2558_2561del	ENSP00000490934.1:p.Tyr853CysfsTer?
ENST00000639389.1:c.151+6651_151+6654del	ENSP00000492572.1:n.151+6651_151+6654del
ENST00000647488.1:c.555_558del	ENSP00000494820.1:n.555_558del
ENST00000675069.1:c.866_869del	ENSP00000502467.1:p.Tyr289CysfsTer?
ENST00000303660.8:c.3332_3335del	ENSP00000302501.4:p.Tyr1111CysfsTer?
ENST00000409487.7:c.3335_3338del	ENSP00000386854.2:p.Tyr1112CysfsTer?
ENST00000419938.5:c.656-879_656-876del	ENSP00000394777.2:n.656-879_656-876del
ENST00000539609.7:c.3263_3266del	ENSP00000443792.2:p.Tyr1088CysfsTer?
ENST00000558170.6:c.3335_3338del	ENSP00000454157.1:p.Tyr1112CysfsTer?
ENST00000627532.2:c.3335_3338del	ENSP00000487174.1:p.Tyr1112CysfsTer?
NM_001171653.1:c.3263_3266del	NP_001165124.1:p.Tyr1088CysfsTer?
NM_014795.3:c.3335_3338del	NP_055610.1:p.Tyr1112CysfsTer?
XM_006712881.2:c.3335_3338del	XP_006712944.1:p.Tyr1112CysfsTer?
XM_006712882.2:c.3335_3338del	XP_006712945.1:p.Tyr1112CysfsTer?
XM_011512231.1:c.3326_3329del	XP_011510533.1:p.Tyr1109CysfsTer?
XM_011512232.1:c.3314_3317del	XP_011510534.1:p.Tyr1105CysfsTer?
NM_014795.4:c.3335_3338del MANE Select	NP_055610.1:p.Tyr1112CysfsTer?
NM_001171653.2:c.3263_3266del	NP_001165124.1:p.Tyr1088CysfsTer?