Canonical Allele Identifier: CA348707826

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1513193
• ClinVar RCV Id: RCV002018340
• dbSNP Id: rs2149876496
• MyVariant Identifiers: chr2:g.145156157T>A (hg19) ; chr2:g.144398590T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398590T>A , CM000664.2:g.144398590T>A	GRCh38
NC_000002.11:g.145156157T>A , CM000664.1:g.145156157T>A	GRCh37
NC_000002.10:g.144872627T>A	NCBI36
NG_016431.1:g.126802A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2446A>T	ENSP00000508434.1:n.*2446A>T
ENST00000440875.6:c.1820A>T	ENSP00000475553.3:p.Lys607Met
ENST00000627532.3:c.2597A>T MANE Select	ENSP00000487174.1:p.Lys866Met
ENST00000636026.2:c.2597A>T	ENSP00000490776.1:p.Lys866Met
ENST00000636179.1:n.2566A>T
ENST00000636413.1:c.2261A>T	ENSP00000490508.1:p.Lys754Met
ENST00000636471.1:c.2672A>T	ENSP00000490317.1:p.Lys891Met
ENST00000636732.2:c.*2314A>T	ENSP00000490175.1:n.*2314A>T
ENST00000636820.1:n.2697A>T
ENST00000637045.1:c.2261A>T	ENSP00000490141.1:p.Lys754Met
ENST00000637304.1:c.2261A>T	ENSP00000490872.1:p.Lys754Met
ENST00000638007.1:c.2261A>T	ENSP00000490723.1:p.Lys754Met
ENST00000638087.1:c.2261A>T	ENSP00000490673.1:p.Lys754Met
ENST00000638128.1:c.1820A>T	ENSP00000490934.1:p.Lys607Met
ENST00000675069.1:c.128A>T	ENSP00000502467.1:p.Lys43Met
ENST00000303660.8:c.2594A>T	ENSP00000302501.4:p.Lys865Met
ENST00000409487.7:c.2597A>T	ENSP00000386854.2:p.Lys866Met
ENST00000419938.5:c.655+2609A>T	ENSP00000394777.2:n.655+2609A>T
ENST00000440875.5:c.1168-662A>T	ENSP00000475553.2:n.1168-662A>T
ENST00000539609.7:c.2525A>T	ENSP00000443792.2:p.Lys842Met
ENST00000558170.6:c.2597A>T	ENSP00000454157.1:p.Lys866Met
ENST00000627532.2:c.2597A>T	ENSP00000487174.1:p.Lys866Met
NM_001171653.1:c.2525A>T	NP_001165124.1:p.Lys842Met
NM_014795.3:c.2597A>T	NP_055610.1:p.Lys866Met
XM_006712881.2:c.2597A>T	XP_006712944.1:p.Lys866Met
XM_006712882.2:c.2597A>T	XP_006712945.1:p.Lys866Met
XM_011512231.1:c.2588A>T	XP_011510533.1:p.Lys863Met
XM_011512232.1:c.2576A>T	XP_011510534.1:p.Lys859Met
NM_014795.4:c.2597A>T MANE Select	NP_055610.1:p.Lys866Met
NM_001171653.2:c.2525A>T	NP_001165124.1:p.Lys842Met