Canonical Allele Identifier: CA348714904

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161640T>A (hg19) ; chr2:g.144404073T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404073T>A , CM000664.2:g.144404073T>A	GRCh38
NC_000002.11:g.145161640T>A , CM000664.1:g.145161640T>A	GRCh37
NC_000002.10:g.144878110T>A	NCBI36
NG_016431.1:g.121319A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*499A>T	ENSP00000508434.1:n.*499A>T
ENST00000440875.6:c.-128A>T	ENSP00000475553.3:n.-128A>T
ENST00000627532.3:c.650A>T MANE Select	ENSP00000487174.1:p.Asp217Val
ENST00000636026.2:c.650A>T	ENSP00000490776.1:p.Asp217Val
ENST00000636179.1:n.619A>T
ENST00000636413.1:c.314A>T	ENSP00000490508.1:p.Asp105Val
ENST00000636471.1:c.650A>T	ENSP00000490317.1:p.Asp217Val
ENST00000636732.2:c.*367A>T	ENSP00000490175.1:n.*367A>T
ENST00000636820.1:n.750A>T
ENST00000637045.1:c.314A>T	ENSP00000490141.1:p.Asp105Val
ENST00000637267.2:c.650A>T	ENSP00000490293.2:p.Asp217Val
ENST00000637304.1:c.314A>T	ENSP00000490872.1:p.Asp105Val
ENST00000638007.1:c.314A>T	ENSP00000490723.1:p.Asp105Val
ENST00000638087.1:c.314A>T	ENSP00000490673.1:p.Asp105Val
ENST00000638128.1:c.-128A>T	ENSP00000490934.1:n.-128A>T
ENST00000675069.1:c.-133-5223A>T	ENSP00000502467.1:n.-133-5223A>T
ENST00000303660.8:c.647A>T	ENSP00000302501.4:p.Asp216Val
ENST00000392861.6:c.734A>T	ENSP00000376601.3:p.Asp245Val
ENST00000409487.7:c.650A>T	ENSP00000386854.2:p.Asp217Val
ENST00000419938.5:c.389A>T	ENSP00000394777.2:p.Asp130Val
ENST00000427902.5:c.737A>T	ENSP00000395496.2:p.Asp246Val
ENST00000440875.5:c.635A>T	ENSP00000475553.2:p.Asp212Val
ENST00000497268.1:n.596A>T
ENST00000539609.7:c.578A>T	ENSP00000443792.2:p.Asp193Val
ENST00000558170.6:c.650A>T	ENSP00000454157.1:p.Asp217Val
ENST00000627532.2:c.650A>T	ENSP00000487174.1:p.Asp217Val
NM_001171653.1:c.578A>T	NP_001165124.1:p.Asp193Val
NM_014795.3:c.650A>T	NP_055610.1:p.Asp217Val
XM_006712881.2:c.650A>T	XP_006712944.1:p.Asp217Val
XM_006712882.2:c.650A>T	XP_006712945.1:p.Asp217Val
XM_011512231.1:c.641A>T	XP_011510533.1:p.Asp214Val
XM_011512232.1:c.629A>T	XP_011510534.1:p.Asp210Val
NM_014795.4:c.650A>T MANE Select	NP_055610.1:p.Asp217Val
NM_001171653.2:c.578A>T	NP_001165124.1:p.Asp193Val