Canonical Allele Identifier: CA348704125

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145154059C>T (hg19) ; chr2:g.144396492C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396492C>T , CM000664.2:g.144396492C>T	GRCh38
NC_000002.11:g.145154059C>T , CM000664.1:g.145154059C>T	GRCh37
NC_000002.10:g.144870529C>T	NCBI36
NG_016431.1:g.128900G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2836G>A	ENSP00000508434.1:n.*2836G>A
ENST00000440875.6:c.2210G>A	ENSP00000475553.3:p.Ser737Asn
ENST00000627532.3:c.2987G>A MANE Select	ENSP00000487174.1:p.Ser996Asn
ENST00000636026.2:c.2987G>A	ENSP00000490776.1:p.Ser996Asn
ENST00000636179.1:n.2956G>A
ENST00000636413.1:c.2651G>A	ENSP00000490508.1:p.Ser884Asn
ENST00000636471.1:c.3062G>A	ENSP00000490317.1:p.Ser1021Asn
ENST00000636732.2:c.*2704G>A	ENSP00000490175.1:n.*2704G>A
ENST00000636820.1:n.3087G>A
ENST00000637045.1:c.2651G>A	ENSP00000490141.1:p.Ser884Asn
ENST00000637304.1:c.2651G>A	ENSP00000490872.1:p.Ser884Asn
ENST00000638007.1:c.2651G>A	ENSP00000490723.1:p.Ser884Asn
ENST00000638087.1:c.2651G>A	ENSP00000490673.1:p.Ser884Asn
ENST00000638128.1:c.2210G>A	ENSP00000490934.1:p.Ser737Asn
ENST00000639389.1:c.71G>A	ENSP00000492572.1:p.Ser24Asn
ENST00000647488.1:c.119G>A	ENSP00000494820.1:p.Ser40Asn
ENST00000675069.1:c.518G>A	ENSP00000502467.1:p.Ser173Asn
ENST00000303660.8:c.2984G>A	ENSP00000302501.4:p.Ser995Asn
ENST00000409487.7:c.2987G>A	ENSP00000386854.2:p.Ser996Asn
ENST00000419938.5:c.655+4707G>A	ENSP00000394777.2:n.655+4707G>A
ENST00000539609.7:c.2915G>A	ENSP00000443792.2:p.Ser972Asn
ENST00000558170.6:c.2987G>A	ENSP00000454157.1:p.Ser996Asn
ENST00000627532.2:c.2987G>A	ENSP00000487174.1:p.Ser996Asn
NM_001171653.1:c.2915G>A	NP_001165124.1:p.Ser972Asn
NM_014795.3:c.2987G>A	NP_055610.1:p.Ser996Asn
XM_006712881.2:c.2987G>A	XP_006712944.1:p.Ser996Asn
XM_006712882.2:c.2987G>A	XP_006712945.1:p.Ser996Asn
XM_011512231.1:c.2978G>A	XP_011510533.1:p.Ser993Asn
XM_011512232.1:c.2966G>A	XP_011510534.1:p.Ser989Asn
NM_014795.4:c.2987G>A MANE Select	NP_055610.1:p.Ser996Asn
NM_001171653.2:c.2915G>A	NP_001165124.1:p.Ser972Asn