Canonical Allele Identifier: CA348707447

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 2762626
• ClinVar RCV Id: RCV003503274
• COSMIC: COSM248438
• MyVariant Identifiers: chr2:g.145156077G>A (hg19) ; chr2:g.144398510G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398510G>A , CM000664.2:g.144398510G>A	GRCh38
NC_000002.11:g.145156077G>A , CM000664.1:g.145156077G>A	GRCh37
NC_000002.10:g.144872547G>A	NCBI36
NG_016431.1:g.126882C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2526C>T	ENSP00000508434.1:n.*2526C>T
ENST00000440875.6:c.1900C>T	ENSP00000475553.3:p.Pro634Ser
ENST00000627532.3:c.2677C>T MANE Select	ENSP00000487174.1:p.Pro893Ser
ENST00000636026.2:c.2677C>T	ENSP00000490776.1:p.Pro893Ser
ENST00000636179.1:n.2646C>T
ENST00000636413.1:c.2341C>T	ENSP00000490508.1:p.Pro781Ser
ENST00000636471.1:c.2752C>T	ENSP00000490317.1:p.Pro918Ser
ENST00000636732.2:c.*2394C>T	ENSP00000490175.1:n.*2394C>T
ENST00000636820.1:n.2777C>T
ENST00000637045.1:c.2341C>T	ENSP00000490141.1:p.Pro781Ser
ENST00000637304.1:c.2341C>T	ENSP00000490872.1:p.Pro781Ser
ENST00000638007.1:c.2341C>T	ENSP00000490723.1:p.Pro781Ser
ENST00000638087.1:c.2341C>T	ENSP00000490673.1:p.Pro781Ser
ENST00000638128.1:c.1900C>T	ENSP00000490934.1:p.Pro634Ser
ENST00000675069.1:c.208C>T	ENSP00000502467.1:p.Pro70Ser
ENST00000303660.8:c.2674C>T	ENSP00000302501.4:p.Pro892Ser
ENST00000409487.7:c.2677C>T	ENSP00000386854.2:p.Pro893Ser
ENST00000419938.5:c.655+2689C>T	ENSP00000394777.2:n.655+2689C>T
ENST00000440875.5:c.1168-582C>T	ENSP00000475553.2:n.1168-582C>T
ENST00000539609.7:c.2605C>T	ENSP00000443792.2:p.Pro869Ser
ENST00000558170.6:c.2677C>T	ENSP00000454157.1:p.Pro893Ser
ENST00000627532.2:c.2677C>T	ENSP00000487174.1:p.Pro893Ser
NM_001171653.1:c.2605C>T	NP_001165124.1:p.Pro869Ser
NM_014795.3:c.2677C>T	NP_055610.1:p.Pro893Ser
XM_006712881.2:c.2677C>T	XP_006712944.1:p.Pro893Ser
XM_006712882.2:c.2677C>T	XP_006712945.1:p.Pro893Ser
XM_011512231.1:c.2668C>T	XP_011510533.1:p.Pro890Ser
XM_011512232.1:c.2656C>T	XP_011510534.1:p.Pro886Ser
NM_014795.4:c.2677C>T MANE Select	NP_055610.1:p.Pro893Ser
NM_001171653.2:c.2605C>T	NP_001165124.1:p.Pro869Ser