Canonical Allele Identifier: CA348714531

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161485G>T (hg19) ; chr2:g.144403918G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403918G>T , CM000664.2:g.144403918G>T	GRCh38
NC_000002.11:g.145161485G>T , CM000664.1:g.145161485G>T	GRCh37
NC_000002.10:g.144877955G>T	NCBI36
NG_016431.1:g.121474C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*654C>A	ENSP00000508434.1:n.*654C>A
ENST00000440875.6:c.28C>A	ENSP00000475553.3:p.Gln10Lys
ENST00000627532.3:c.805C>A MANE Select	ENSP00000487174.1:p.Gln269Lys
ENST00000636026.2:c.805C>A	ENSP00000490776.1:p.Gln269Lys
ENST00000636179.1:n.774C>A
ENST00000636413.1:c.469C>A	ENSP00000490508.1:p.Gln157Lys
ENST00000636471.1:c.805C>A	ENSP00000490317.1:p.Gln269Lys
ENST00000636732.2:c.*522C>A	ENSP00000490175.1:n.*522C>A
ENST00000636820.1:n.905C>A
ENST00000637045.1:c.469C>A	ENSP00000490141.1:p.Gln157Lys
ENST00000637267.2:c.805C>A	ENSP00000490293.2:p.Gln269Lys
ENST00000637304.1:c.469C>A	ENSP00000490872.1:p.Gln157Lys
ENST00000638007.1:c.469C>A	ENSP00000490723.1:p.Gln157Lys
ENST00000638087.1:c.469C>A	ENSP00000490673.1:p.Gln157Lys
ENST00000638128.1:c.28C>A	ENSP00000490934.1:p.Gln10Lys
ENST00000675069.1:c.-133-5068C>A	ENSP00000502467.1:n.-133-5068C>A
ENST00000303660.8:c.802C>A	ENSP00000302501.4:p.Gln268Lys
ENST00000392861.6:c.889C>A	ENSP00000376601.3:p.Gln297Lys
ENST00000409487.7:c.805C>A	ENSP00000386854.2:p.Gln269Lys
ENST00000419938.5:c.544C>A	ENSP00000394777.2:p.Gln182Lys
ENST00000427902.5:c.892C>A	ENSP00000395496.2:p.Gln298Lys
ENST00000440875.5:c.790C>A	ENSP00000475553.2:p.Gln264Lys
ENST00000539609.7:c.733C>A	ENSP00000443792.2:p.Gln245Lys
ENST00000558170.6:c.805C>A	ENSP00000454157.1:p.Gln269Lys
ENST00000627532.2:c.805C>A	ENSP00000487174.1:p.Gln269Lys
NM_001171653.1:c.733C>A	NP_001165124.1:p.Gln245Lys
NM_014795.3:c.805C>A	NP_055610.1:p.Gln269Lys
XM_006712881.2:c.805C>A	XP_006712944.1:p.Gln269Lys
XM_006712882.2:c.805C>A	XP_006712945.1:p.Gln269Lys
XM_011512231.1:c.796C>A	XP_011510533.1:p.Gln266Lys
XM_011512232.1:c.784C>A	XP_011510534.1:p.Gln262Lys
NM_014795.4:c.805C>A MANE Select	NP_055610.1:p.Gln269Lys
NM_001171653.2:c.733C>A	NP_001165124.1:p.Gln245Lys