Canonical Allele Identifier: CA348714891

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161634C>A (hg19) ; chr2:g.144404067C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404067C>A , CM000664.2:g.144404067C>A	GRCh38
NC_000002.11:g.145161634C>A , CM000664.1:g.145161634C>A	GRCh37
NC_000002.10:g.144878104C>A	NCBI36
NG_016431.1:g.121325G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*505G>T	ENSP00000508434.1:n.*505G>T
ENST00000440875.6:c.-122G>T	ENSP00000475553.3:n.-122G>T
ENST00000627532.3:c.656G>T MANE Select	ENSP00000487174.1:p.Gly219Val
ENST00000636026.2:c.656G>T	ENSP00000490776.1:p.Gly219Val
ENST00000636179.1:n.625G>T
ENST00000636413.1:c.320G>T	ENSP00000490508.1:p.Gly107Val
ENST00000636471.1:c.656G>T	ENSP00000490317.1:p.Gly219Val
ENST00000636732.2:c.*373G>T	ENSP00000490175.1:n.*373G>T
ENST00000636820.1:n.756G>T
ENST00000637045.1:c.320G>T	ENSP00000490141.1:p.Gly107Val
ENST00000637267.2:c.656G>T	ENSP00000490293.2:p.Gly219Val
ENST00000637304.1:c.320G>T	ENSP00000490872.1:p.Gly107Val
ENST00000638007.1:c.320G>T	ENSP00000490723.1:p.Gly107Val
ENST00000638087.1:c.320G>T	ENSP00000490673.1:p.Gly107Val
ENST00000638128.1:c.-122G>T	ENSP00000490934.1:n.-122G>T
ENST00000675069.1:c.-133-5217G>T	ENSP00000502467.1:n.-133-5217G>T
ENST00000303660.8:c.653G>T	ENSP00000302501.4:p.Gly218Val
ENST00000392861.6:c.740G>T	ENSP00000376601.3:p.Gly247Val
ENST00000409487.7:c.656G>T	ENSP00000386854.2:p.Gly219Val
ENST00000419938.5:c.395G>T	ENSP00000394777.2:p.Gly132Val
ENST00000427902.5:c.743G>T	ENSP00000395496.2:p.Gly248Val
ENST00000440875.5:c.641G>T	ENSP00000475553.2:p.Gly214Val
ENST00000497268.1:n.602G>T
ENST00000539609.7:c.584G>T	ENSP00000443792.2:p.Gly195Val
ENST00000558170.6:c.656G>T	ENSP00000454157.1:p.Gly219Val
ENST00000627532.2:c.656G>T	ENSP00000487174.1:p.Gly219Val
NM_001171653.1:c.584G>T	NP_001165124.1:p.Gly195Val
NM_014795.3:c.656G>T	NP_055610.1:p.Gly219Val
XM_006712881.2:c.656G>T	XP_006712944.1:p.Gly219Val
XM_006712882.2:c.656G>T	XP_006712945.1:p.Gly219Val
XM_011512231.1:c.647G>T	XP_011510533.1:p.Gly216Val
XM_011512232.1:c.635G>T	XP_011510534.1:p.Gly212Val
NM_014795.4:c.656G>T MANE Select	NP_055610.1:p.Gly219Val
NM_001171653.2:c.584G>T	NP_001165124.1:p.Gly195Val