Canonical Allele Identifier: CA348714850

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161613A>C (hg19) ; chr2:g.144404046A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404046A>C , CM000664.2:g.144404046A>C	GRCh38
NC_000002.11:g.145161613A>C , CM000664.1:g.145161613A>C	GRCh37
NC_000002.10:g.144878083A>C	NCBI36
NG_016431.1:g.121346T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*526T>G	ENSP00000508434.1:n.*526T>G
ENST00000440875.6:c.-101T>G	ENSP00000475553.3:n.-101T>G
ENST00000627532.3:c.677T>G MANE Select	ENSP00000487174.1:p.Leu226Arg
ENST00000636026.2:c.677T>G	ENSP00000490776.1:p.Leu226Arg
ENST00000636179.1:n.646T>G
ENST00000636413.1:c.341T>G	ENSP00000490508.1:p.Leu114Arg
ENST00000636471.1:c.677T>G	ENSP00000490317.1:p.Leu226Arg
ENST00000636732.2:c.*394T>G	ENSP00000490175.1:n.*394T>G
ENST00000636820.1:n.777T>G
ENST00000637045.1:c.341T>G	ENSP00000490141.1:p.Leu114Arg
ENST00000637267.2:c.677T>G	ENSP00000490293.2:p.Leu226Arg
ENST00000637304.1:c.341T>G	ENSP00000490872.1:p.Leu114Arg
ENST00000638007.1:c.341T>G	ENSP00000490723.1:p.Leu114Arg
ENST00000638087.1:c.341T>G	ENSP00000490673.1:p.Leu114Arg
ENST00000638128.1:c.-101T>G	ENSP00000490934.1:n.-101T>G
ENST00000675069.1:c.-133-5196T>G	ENSP00000502467.1:n.-133-5196T>G
ENST00000303660.8:c.674T>G	ENSP00000302501.4:p.Leu225Arg
ENST00000392861.6:c.761T>G	ENSP00000376601.3:p.Leu254Arg
ENST00000409487.7:c.677T>G	ENSP00000386854.2:p.Leu226Arg
ENST00000419938.5:c.416T>G	ENSP00000394777.2:p.Leu139Arg
ENST00000427902.5:c.764T>G	ENSP00000395496.2:p.Leu255Arg
ENST00000440875.5:c.662T>G	ENSP00000475553.2:p.Leu221Arg
ENST00000497268.1:n.623T>G
ENST00000539609.7:c.605T>G	ENSP00000443792.2:p.Leu202Arg
ENST00000558170.6:c.677T>G	ENSP00000454157.1:p.Leu226Arg
ENST00000627532.2:c.677T>G	ENSP00000487174.1:p.Leu226Arg
NM_001171653.1:c.605T>G	NP_001165124.1:p.Leu202Arg
NM_014795.3:c.677T>G	NP_055610.1:p.Leu226Arg
XM_006712881.2:c.677T>G	XP_006712944.1:p.Leu226Arg
XM_006712882.2:c.677T>G	XP_006712945.1:p.Leu226Arg
XM_011512231.1:c.668T>G	XP_011510533.1:p.Leu223Arg
XM_011512232.1:c.656T>G	XP_011510534.1:p.Leu219Arg
NM_014795.4:c.677T>G MANE Select	NP_055610.1:p.Leu226Arg
NM_001171653.2:c.605T>G	NP_001165124.1:p.Leu202Arg