Canonical Allele Identifier: CA348714706

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161553C>A (hg19) ; chr2:g.144403986C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403986C>A , CM000664.2:g.144403986C>A	GRCh38
NC_000002.11:g.145161553C>A , CM000664.1:g.145161553C>A	GRCh37
NC_000002.10:g.144878023C>A	NCBI36
NG_016431.1:g.121406G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*586G>T	ENSP00000508434.1:n.*586G>T
ENST00000440875.6:c.-41G>T	ENSP00000475553.3:n.-41G>T
ENST00000627532.3:c.737G>T MANE Select	ENSP00000487174.1:p.Cys246Phe
ENST00000636026.2:c.737G>T	ENSP00000490776.1:p.Cys246Phe
ENST00000636179.1:n.706G>T
ENST00000636413.1:c.401G>T	ENSP00000490508.1:p.Cys134Phe
ENST00000636471.1:c.737G>T	ENSP00000490317.1:p.Cys246Phe
ENST00000636732.2:c.*454G>T	ENSP00000490175.1:n.*454G>T
ENST00000636820.1:n.837G>T
ENST00000637045.1:c.401G>T	ENSP00000490141.1:p.Cys134Phe
ENST00000637267.2:c.737G>T	ENSP00000490293.2:p.Cys246Phe
ENST00000637304.1:c.401G>T	ENSP00000490872.1:p.Cys134Phe
ENST00000638007.1:c.401G>T	ENSP00000490723.1:p.Cys134Phe
ENST00000638087.1:c.401G>T	ENSP00000490673.1:p.Cys134Phe
ENST00000638128.1:c.-41G>T	ENSP00000490934.1:n.-41G>T
ENST00000675069.1:c.-133-5136G>T	ENSP00000502467.1:n.-133-5136G>T
ENST00000303660.8:c.734G>T	ENSP00000302501.4:p.Cys245Phe
ENST00000392861.6:c.821G>T	ENSP00000376601.3:p.Cys274Phe
ENST00000409487.7:c.737G>T	ENSP00000386854.2:p.Cys246Phe
ENST00000419938.5:c.476G>T	ENSP00000394777.2:p.Cys159Phe
ENST00000427902.5:c.824G>T	ENSP00000395496.2:p.Cys275Phe
ENST00000440875.5:c.722G>T	ENSP00000475553.2:p.Cys241Phe
ENST00000539609.7:c.665G>T	ENSP00000443792.2:p.Cys222Phe
ENST00000558170.6:c.737G>T	ENSP00000454157.1:p.Cys246Phe
ENST00000627532.2:c.737G>T	ENSP00000487174.1:p.Cys246Phe
NM_001171653.1:c.665G>T	NP_001165124.1:p.Cys222Phe
NM_014795.3:c.737G>T	NP_055610.1:p.Cys246Phe
XM_006712881.2:c.737G>T	XP_006712944.1:p.Cys246Phe
XM_006712882.2:c.737G>T	XP_006712945.1:p.Cys246Phe
XM_011512231.1:c.728G>T	XP_011510533.1:p.Cys243Phe
XM_011512232.1:c.716G>T	XP_011510534.1:p.Cys239Phe
NM_014795.4:c.737G>T MANE Select	NP_055610.1:p.Cys246Phe
NM_001171653.2:c.665G>T	NP_001165124.1:p.Cys222Phe