Canonical Allele Identifier: CA429441174

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147297_145147315delAGAGTACCCCTGAGGGGTA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389731_144389749del , CM000664.2:g.144389731_144389749del	GRCh38
NC_000002.11:g.145147298_145147316del , CM000664.1:g.145147298_145147316del	GRCh37
NC_000002.10:g.144863768_144863786del	NCBI36
NG_016431.1:g.135644_135662del

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3197_*3215del	ENSP00000508434.1:n.*3197_*3215del
ENST00000440875.6:c.2571_2589del	ENSP00000475553.3:p.Ile857MetfsTer?
ENST00000627532.3:c.3348_3366del MANE Select	ENSP00000487174.1:p.Ile1116MetfsTer?
ENST00000636026.2:c.3236_3254del	ENSP00000490776.1:p.Leu1079Ter
ENST00000636179.1:n.3317_3335del
ENST00000636413.1:c.3012_3030del	ENSP00000490508.1:p.Ile1004MetfsTer?
ENST00000636471.1:c.3423_3441del	ENSP00000490317.1:p.Ile1141MetfsTer?
ENST00000636732.2:c.*3065_*3083del	ENSP00000490175.1:n.*3065_*3083del
ENST00000636820.1:n.3448_3466del
ENST00000637045.1:c.3012_3030del	ENSP00000490141.1:p.Ile1004MetfsTer?
ENST00000637304.1:c.3012_3030del	ENSP00000490872.1:p.Ile1004MetfsTer?
ENST00000638007.1:c.3012_3030del	ENSP00000490723.1:p.Ile1004MetfsTer?
ENST00000638087.1:c.3012_3030del	ENSP00000490673.1:p.Ile1004MetfsTer?
ENST00000638128.1:c.2571_2589del	ENSP00000490934.1:p.Ile857MetfsTer?
ENST00000639389.1:c.151+6664_151+6682del	ENSP00000492572.1:n.151+6664_151+6682del
ENST00000647488.1:c.568_586del	ENSP00000494820.1:n.568_586del
ENST00000675069.1:c.879_897del	ENSP00000502467.1:p.Ile293MetfsTer?
ENST00000303660.8:c.3345_3363del	ENSP00000302501.4:p.Ile1115MetfsTer?
ENST00000409487.7:c.3348_3366del	ENSP00000386854.2:p.Ile1116MetfsTer?
ENST00000419938.5:c.656-866_656-848del	ENSP00000394777.2:n.656-866_656-848del
ENST00000539609.7:c.3276_3294del	ENSP00000443792.2:p.Ile1092MetfsTer?
ENST00000558170.6:c.3348_3366del	ENSP00000454157.1:p.Ile1116MetfsTer?
ENST00000627532.2:c.3348_3366del	ENSP00000487174.1:p.Ile1116MetfsTer?
NM_001171653.1:c.3276_3294del	NP_001165124.1:p.Ile1092MetfsTer?
NM_014795.3:c.3348_3366del	NP_055610.1:p.Ile1116MetfsTer?
XM_006712881.2:c.3348_3366del	XP_006712944.1:p.Ile1116MetfsTer?
XM_006712882.2:c.3348_3366del	XP_006712945.1:p.Ile1116MetfsTer?
XM_011512231.1:c.3339_3357del	XP_011510533.1:p.Ile1113MetfsTer?
XM_011512232.1:c.3327_3345del	XP_011510534.1:p.Ile1109MetfsTer?
NM_014795.4:c.3348_3366del MANE Select	NP_055610.1:p.Ile1116MetfsTer?
NM_001171653.2:c.3276_3294del	NP_001165124.1:p.Ile1092MetfsTer?