Canonical Allele Identifier: CA348712131

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145157441T>C (hg19) ; chr2:g.144399874T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399874T>C , CM000664.2:g.144399874T>C	GRCh38
NC_000002.11:g.145157441T>C , CM000664.1:g.145157441T>C	GRCh37
NC_000002.10:g.144873911T>C	NCBI36
NG_016431.1:g.125518A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1162A>G	ENSP00000508434.1:n.*1162A>G
ENST00000440875.6:c.536A>G	ENSP00000475553.3:p.His179Arg
ENST00000627532.3:c.1313A>G MANE Select	ENSP00000487174.1:p.His438Arg
ENST00000636026.2:c.1313A>G	ENSP00000490776.1:p.His438Arg
ENST00000636179.1:n.1282A>G
ENST00000636413.1:c.977A>G	ENSP00000490508.1:p.His326Arg
ENST00000636471.1:c.1388A>G	ENSP00000490317.1:p.His463Arg
ENST00000636732.2:c.*1030A>G	ENSP00000490175.1:n.*1030A>G
ENST00000636820.1:n.1413A>G
ENST00000637045.1:c.977A>G	ENSP00000490141.1:p.His326Arg
ENST00000637267.2:c.1313A>G	ENSP00000490293.2:p.His438Arg
ENST00000637304.1:c.977A>G	ENSP00000490872.1:p.His326Arg
ENST00000638007.1:c.977A>G	ENSP00000490723.1:p.His326Arg
ENST00000638087.1:c.977A>G	ENSP00000490673.1:p.His326Arg
ENST00000638128.1:c.536A>G	ENSP00000490934.1:p.His179Arg
ENST00000675069.1:c.-133-1024A>G	ENSP00000502467.1:n.-133-1024A>G
ENST00000675145.1:n.1861A>G
ENST00000303660.8:c.1310A>G	ENSP00000302501.4:p.His437Arg
ENST00000392861.6:c.1397A>G	ENSP00000376601.3:p.His466Arg
ENST00000409487.7:c.1313A>G	ENSP00000386854.2:p.His438Arg
ENST00000419938.5:c.655+1325A>G	ENSP00000394777.2:n.655+1325A>G
ENST00000427902.5:c.1400A>G	ENSP00000395496.2:p.His467Arg
ENST00000440875.5:c.1153+145A>G	ENSP00000475553.2:n.1153+145A>G
ENST00000539609.7:c.1241A>G	ENSP00000443792.2:p.His414Arg
ENST00000558170.6:c.1313A>G	ENSP00000454157.1:p.His438Arg
ENST00000627532.2:c.1313A>G	ENSP00000487174.1:p.His438Arg
NM_001171653.1:c.1241A>G	NP_001165124.1:p.His414Arg
NM_014795.3:c.1313A>G	NP_055610.1:p.His438Arg
XM_006712881.2:c.1313A>G	XP_006712944.1:p.His438Arg
XM_006712882.2:c.1313A>G	XP_006712945.1:p.His438Arg
XM_011512231.1:c.1304A>G	XP_011510533.1:p.His435Arg
XM_011512232.1:c.1292A>G	XP_011510534.1:p.His431Arg
NM_014795.4:c.1313A>G MANE Select	NP_055610.1:p.His438Arg
NM_001171653.2:c.1241A>G	NP_001165124.1:p.His414Arg