Canonical Allele Identifier: CA348699095

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147140C>T (hg19) ; chr2:g.144389573C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389573C>T , CM000664.2:g.144389573C>T	GRCh38
NC_000002.11:g.145147140C>T , CM000664.1:g.145147140C>T	GRCh37
NC_000002.10:g.144863610C>T	NCBI36
NG_016431.1:g.135819G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3372G>A	ENSP00000508434.1:n.*3372G>A
ENST00000440875.6:c.2746G>A	ENSP00000475553.3:p.Asp916Asn
ENST00000627532.3:c.3523G>A MANE Select	ENSP00000487174.1:p.Asp1175Asn
ENST00000636026.2:c.3411G>A	ENSP00000490776.1:p.Arg1137=
ENST00000636179.1:n.3492G>A
ENST00000636413.1:c.3187G>A	ENSP00000490508.1:p.Asp1063Asn
ENST00000636471.1:c.3598G>A	ENSP00000490317.1:p.Asp1200Asn
ENST00000636732.2:c.*3240G>A	ENSP00000490175.1:n.*3240G>A
ENST00000636820.1:n.3623G>A
ENST00000637045.1:c.3187G>A	ENSP00000490141.1:p.Asp1063Asn
ENST00000637304.1:c.3187G>A	ENSP00000490872.1:p.Asp1063Asn
ENST00000638007.1:c.3187G>A	ENSP00000490723.1:p.Asp1063Asn
ENST00000638087.1:c.3187G>A	ENSP00000490673.1:p.Asp1063Asn
ENST00000638128.1:c.2746G>A	ENSP00000490934.1:p.Asp916Asn
ENST00000639389.1:c.151+6839G>A	ENSP00000492572.1:n.151+6839G>A
ENST00000647488.1:c.743G>A	ENSP00000494820.1:n.743G>A
ENST00000675069.1:c.1054G>A	ENSP00000502467.1:p.Asp352Asn
ENST00000303660.8:c.3520G>A	ENSP00000302501.4:p.Asp1174Asn
ENST00000409487.7:c.3523G>A	ENSP00000386854.2:p.Asp1175Asn
ENST00000419938.5:c.656-691G>A	ENSP00000394777.2:n.656-691G>A
ENST00000539609.7:c.3451G>A	ENSP00000443792.2:p.Asp1151Asn
ENST00000558170.6:c.3523G>A	ENSP00000454157.1:p.Asp1175Asn
ENST00000627532.2:c.3523G>A	ENSP00000487174.1:p.Asp1175Asn
NM_001171653.1:c.3451G>A	NP_001165124.1:p.Asp1151Asn
NM_014795.3:c.3523G>A	NP_055610.1:p.Asp1175Asn
XM_006712881.2:c.3523G>A	XP_006712944.1:p.Asp1175Asn
XM_006712882.2:c.3523G>A	XP_006712945.1:p.Asp1175Asn
XM_011512231.1:c.3514G>A	XP_011510533.1:p.Asp1172Asn
XM_011512232.1:c.3502G>A	XP_011510534.1:p.Asp1168Asn
NM_014795.4:c.3523G>A MANE Select	NP_055610.1:p.Asp1175Asn
NM_001171653.2:c.3451G>A	NP_001165124.1:p.Asp1151Asn