Canonical Allele Identifier: CA348706925

Gene: ZEB2

Linked Data

• COSMIC: COSM3364296
• MyVariant Identifiers: chr2:g.145155963A>C (hg19) ; chr2:g.144398396A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398396A>C , CM000664.2:g.144398396A>C	GRCh38
NC_000002.11:g.145155963A>C , CM000664.1:g.145155963A>C	GRCh37
NC_000002.10:g.144872433A>C	NCBI36
NG_016431.1:g.126996T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2640T>G	ENSP00000508434.1:n.*2640T>G
ENST00000440875.6:c.2014T>G	ENSP00000475553.3:p.Phe672Val
ENST00000627532.3:c.2791T>G MANE Select	ENSP00000487174.1:p.Phe931Val
ENST00000636026.2:c.2791T>G	ENSP00000490776.1:p.Phe931Val
ENST00000636179.1:n.2760T>G
ENST00000636413.1:c.2455T>G	ENSP00000490508.1:p.Phe819Val
ENST00000636471.1:c.2866T>G	ENSP00000490317.1:p.Phe956Val
ENST00000636732.2:c.*2508T>G	ENSP00000490175.1:n.*2508T>G
ENST00000636820.1:n.2891T>G
ENST00000637045.1:c.2455T>G	ENSP00000490141.1:p.Phe819Val
ENST00000637304.1:c.2455T>G	ENSP00000490872.1:p.Phe819Val
ENST00000638007.1:c.2455T>G	ENSP00000490723.1:p.Phe819Val
ENST00000638087.1:c.2455T>G	ENSP00000490673.1:p.Phe819Val
ENST00000638128.1:c.2014T>G	ENSP00000490934.1:p.Phe672Val
ENST00000675069.1:c.322T>G	ENSP00000502467.1:p.Phe108Val
ENST00000303660.8:c.2788T>G	ENSP00000302501.4:p.Phe930Val
ENST00000409487.7:c.2791T>G	ENSP00000386854.2:p.Phe931Val
ENST00000419938.5:c.655+2803T>G	ENSP00000394777.2:n.655+2803T>G
ENST00000440875.5:c.1168-468T>G	ENSP00000475553.2:n.1168-468T>G
ENST00000539609.7:c.2719T>G	ENSP00000443792.2:p.Phe907Val
ENST00000558170.6:c.2791T>G	ENSP00000454157.1:p.Phe931Val
ENST00000627532.2:c.2791T>G	ENSP00000487174.1:p.Phe931Val
NM_001171653.1:c.2719T>G	NP_001165124.1:p.Phe907Val
NM_014795.3:c.2791T>G	NP_055610.1:p.Phe931Val
XM_006712881.2:c.2791T>G	XP_006712944.1:p.Phe931Val
XM_006712882.2:c.2791T>G	XP_006712945.1:p.Phe931Val
XM_011512231.1:c.2782T>G	XP_011510533.1:p.Phe928Val
XM_011512232.1:c.2770T>G	XP_011510534.1:p.Phe924Val
NM_014795.4:c.2791T>G MANE Select	NP_055610.1:p.Phe931Val
NM_001171653.2:c.2719T>G	NP_001165124.1:p.Phe907Val