Canonical Allele Identifier: CA348710181

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156965G>A (hg19) ; chr2:g.144399398G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399398G>A , CM000664.2:g.144399398G>A	GRCh38
NC_000002.11:g.145156965G>A , CM000664.1:g.145156965G>A	GRCh37
NC_000002.10:g.144873435G>A	NCBI36
NG_016431.1:g.125994C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1638C>T	ENSP00000508434.1:n.*1638C>T
ENST00000440875.6:c.1012C>T	ENSP00000475553.3:p.His338Tyr
ENST00000627532.3:c.1789C>T MANE Select	ENSP00000487174.1:p.His597Tyr
ENST00000636026.2:c.1789C>T	ENSP00000490776.1:p.His597Tyr
ENST00000636179.1:n.1758C>T
ENST00000636413.1:c.1453C>T	ENSP00000490508.1:p.His485Tyr
ENST00000636471.1:c.1864C>T	ENSP00000490317.1:p.His622Tyr
ENST00000636732.2:c.*1506C>T	ENSP00000490175.1:n.*1506C>T
ENST00000636820.1:n.1889C>T
ENST00000637045.1:c.1453C>T	ENSP00000490141.1:p.His485Tyr
ENST00000637267.2:c.1789C>T	ENSP00000490293.2:p.His597Tyr
ENST00000637304.1:c.1453C>T	ENSP00000490872.1:p.His485Tyr
ENST00000638007.1:c.1453C>T	ENSP00000490723.1:p.His485Tyr
ENST00000638087.1:c.1453C>T	ENSP00000490673.1:p.His485Tyr
ENST00000638128.1:c.1012C>T	ENSP00000490934.1:p.His338Tyr
ENST00000675069.1:c.-133-548C>T	ENSP00000502467.1:n.-133-548C>T
ENST00000675145.1:n.2337C>T
ENST00000303660.8:c.1786C>T	ENSP00000302501.4:p.His596Tyr
ENST00000409487.7:c.1789C>T	ENSP00000386854.2:p.His597Tyr
ENST00000419938.5:c.655+1801C>T	ENSP00000394777.2:n.655+1801C>T
ENST00000427902.5:c.1876C>T	ENSP00000395496.2:p.His626Tyr
ENST00000440875.5:c.1167+139C>T	ENSP00000475553.2:n.1167+139C>T
ENST00000539609.7:c.1717C>T	ENSP00000443792.2:p.His573Tyr
ENST00000558170.6:c.1789C>T	ENSP00000454157.1:p.His597Tyr
ENST00000627532.2:c.1789C>T	ENSP00000487174.1:p.His597Tyr
NM_001171653.1:c.1717C>T	NP_001165124.1:p.His573Tyr
NM_014795.3:c.1789C>T	NP_055610.1:p.His597Tyr
XM_006712881.2:c.1789C>T	XP_006712944.1:p.His597Tyr
XM_006712882.2:c.1789C>T	XP_006712945.1:p.His597Tyr
XM_011512231.1:c.1780C>T	XP_011510533.1:p.His594Tyr
XM_011512232.1:c.1768C>T	XP_011510534.1:p.His590Tyr
NM_014795.4:c.1789C>T MANE Select	NP_055610.1:p.His597Tyr
NM_001171653.2:c.1717C>T	NP_001165124.1:p.His573Tyr