Canonical Allele Identifier: CA429218504

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161546_145161547insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403979_144403980insA , CM000664.2:g.144403979_144403980insA	GRCh38
NC_000002.11:g.145161546_145161547insA , CM000664.1:g.145161546_145161547insA	GRCh37
NC_000002.10:g.144878016_144878017insA	NCBI36
NG_016431.1:g.121412_121413insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*592_*593insT	ENSP00000508434.1:n.*592_*593insT
ENST00000440875.6:c.-35_-34insT	ENSP00000475553.3:n.-35_-34insT
ENST00000627532.3:c.743_744insT MANE Select	ENSP00000487174.1:p.Thr249HisfsTer?
ENST00000636026.2:c.743_744insT	ENSP00000490776.1:p.Thr249HisfsTer?
ENST00000636179.1:n.712_713insT
ENST00000636413.1:c.407_408insT	ENSP00000490508.1:p.Thr137HisfsTer?
ENST00000636471.1:c.743_744insT	ENSP00000490317.1:p.Thr249HisfsTer?
ENST00000636732.2:c.*460_*461insT	ENSP00000490175.1:n.*460_*461insT
ENST00000636820.1:n.843_844insT
ENST00000637045.1:c.407_408insT	ENSP00000490141.1:p.Thr137HisfsTer?
ENST00000637267.2:c.743_744insT	ENSP00000490293.2:p.Thr249HisfsTer?
ENST00000637304.1:c.407_408insT	ENSP00000490872.1:p.Thr137HisfsTer?
ENST00000638007.1:c.407_408insT	ENSP00000490723.1:p.Thr137HisfsTer?
ENST00000638087.1:c.407_408insT	ENSP00000490673.1:p.Thr137HisfsTer?
ENST00000638128.1:c.-35_-34insT	ENSP00000490934.1:n.-35_-34insT
ENST00000675069.1:c.-133-5130_-133-5129insT	ENSP00000502467.1:n.-133-5130_-133-5129in...
ENST00000303660.8:c.740_741insT	ENSP00000302501.4:p.Thr248HisfsTer?
ENST00000392861.6:c.827_828insT	ENSP00000376601.3:p.Thr277HisfsTer?
ENST00000409487.7:c.743_744insT	ENSP00000386854.2:p.Thr249HisfsTer?
ENST00000419938.5:c.482_483insT	ENSP00000394777.2:p.Thr162HisfsTer?
ENST00000427902.5:c.830_831insT	ENSP00000395496.2:p.Thr278HisfsTer?
ENST00000440875.5:c.728_729insT	ENSP00000475553.2:p.Thr244HisfsTer?
ENST00000539609.7:c.671_672insT	ENSP00000443792.2:p.Thr225HisfsTer?
ENST00000558170.6:c.743_744insT	ENSP00000454157.1:p.Thr249HisfsTer?
ENST00000627532.2:c.743_744insT	ENSP00000487174.1:p.Thr249HisfsTer?
NM_001171653.1:c.671_672insT	NP_001165124.1:p.Thr225HisfsTer?
NM_014795.3:c.743_744insT	NP_055610.1:p.Thr249HisfsTer?
XM_006712881.2:c.743_744insT	XP_006712944.1:p.Thr249HisfsTer?
XM_006712882.2:c.743_744insT	XP_006712945.1:p.Thr249HisfsTer?
XM_011512231.1:c.734_735insT	XP_011510533.1:p.Thr246HisfsTer?
XM_011512232.1:c.722_723insT	XP_011510534.1:p.Thr242HisfsTer?
NM_014795.4:c.743_744insT MANE Select	NP_055610.1:p.Thr249HisfsTer?
NM_001171653.2:c.671_672insT	NP_001165124.1:p.Thr225HisfsTer?