Canonical Allele Identifier: CA429445138

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156108T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398541T>G , CM000664.2:g.144398541T>G	GRCh38
NC_000002.11:g.145156108T>G , CM000664.1:g.145156108T>G	GRCh37
NC_000002.10:g.144872578T>G	NCBI36
NG_016431.1:g.126851A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2495A>C	ENSP00000508434.1:n.*2495A>C
ENST00000440875.6:c.1869A>C	ENSP00000475553.3:p.Pro623=
ENST00000627532.3:c.2646A>C MANE Select	ENSP00000487174.1:p.Pro882=
ENST00000636026.2:c.2646A>C	ENSP00000490776.1:p.Pro882=
ENST00000636179.1:n.2615A>C
ENST00000636413.1:c.2310A>C	ENSP00000490508.1:p.Pro770=
ENST00000636471.1:c.2721A>C	ENSP00000490317.1:p.Pro907=
ENST00000636732.2:c.*2363A>C	ENSP00000490175.1:n.*2363A>C
ENST00000636820.1:n.2746A>C
ENST00000637045.1:c.2310A>C	ENSP00000490141.1:p.Pro770=
ENST00000637304.1:c.2310A>C	ENSP00000490872.1:p.Pro770=
ENST00000638007.1:c.2310A>C	ENSP00000490723.1:p.Pro770=
ENST00000638087.1:c.2310A>C	ENSP00000490673.1:p.Pro770=
ENST00000638128.1:c.1869A>C	ENSP00000490934.1:p.Pro623=
ENST00000675069.1:c.177A>C	ENSP00000502467.1:p.Pro59=
ENST00000303660.8:c.2643A>C	ENSP00000302501.4:p.Pro881=
ENST00000409487.7:c.2646A>C	ENSP00000386854.2:p.Pro882=
ENST00000419938.5:c.655+2658A>C	ENSP00000394777.2:n.655+2658A>C
ENST00000440875.5:c.1168-613A>C	ENSP00000475553.2:n.1168-613A>C
ENST00000539609.7:c.2574A>C	ENSP00000443792.2:p.Pro858=
ENST00000558170.6:c.2646A>C	ENSP00000454157.1:p.Pro882=
ENST00000627532.2:c.2646A>C	ENSP00000487174.1:p.Pro882=
NM_001171653.1:c.2574A>C	NP_001165124.1:p.Pro858=
NM_014795.3:c.2646A>C	NP_055610.1:p.Pro882=
XM_006712881.2:c.2646A>C	XP_006712944.1:p.Pro882=
XM_006712882.2:c.2646A>C	XP_006712945.1:p.Pro882=
XM_011512231.1:c.2637A>C	XP_011510533.1:p.Pro879=
XM_011512232.1:c.2625A>C	XP_011510534.1:p.Pro875=
NM_014795.4:c.2646A>C MANE Select	NP_055610.1:p.Pro882=
NM_001171653.2:c.2574A>C	NP_001165124.1:p.Pro858=