Canonical Allele Identifier: CA348714749

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161572T>A (hg19) ; chr2:g.144404005T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404005T>A , CM000664.2:g.144404005T>A	GRCh38
NC_000002.11:g.145161572T>A , CM000664.1:g.145161572T>A	GRCh37
NC_000002.10:g.144878042T>A	NCBI36
NG_016431.1:g.121387A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*567A>T	ENSP00000508434.1:n.*567A>T
ENST00000440875.6:c.-60A>T	ENSP00000475553.3:n.-60A>T
ENST00000627532.3:c.718A>T MANE Select	ENSP00000487174.1:p.Asn240Tyr
ENST00000636026.2:c.718A>T	ENSP00000490776.1:p.Asn240Tyr
ENST00000636179.1:n.687A>T
ENST00000636413.1:c.382A>T	ENSP00000490508.1:p.Asn128Tyr
ENST00000636471.1:c.718A>T	ENSP00000490317.1:p.Asn240Tyr
ENST00000636732.2:c.*435A>T	ENSP00000490175.1:n.*435A>T
ENST00000636820.1:n.818A>T
ENST00000637045.1:c.382A>T	ENSP00000490141.1:p.Asn128Tyr
ENST00000637267.2:c.718A>T	ENSP00000490293.2:p.Asn240Tyr
ENST00000637304.1:c.382A>T	ENSP00000490872.1:p.Asn128Tyr
ENST00000638007.1:c.382A>T	ENSP00000490723.1:p.Asn128Tyr
ENST00000638087.1:c.382A>T	ENSP00000490673.1:p.Asn128Tyr
ENST00000638128.1:c.-60A>T	ENSP00000490934.1:n.-60A>T
ENST00000675069.1:c.-133-5155A>T	ENSP00000502467.1:n.-133-5155A>T
ENST00000303660.8:c.715A>T	ENSP00000302501.4:p.Asn239Tyr
ENST00000392861.6:c.802A>T	ENSP00000376601.3:p.Asn268Tyr
ENST00000409487.7:c.718A>T	ENSP00000386854.2:p.Asn240Tyr
ENST00000419938.5:c.457A>T	ENSP00000394777.2:p.Asn153Tyr
ENST00000427902.5:c.805A>T	ENSP00000395496.2:p.Asn269Tyr
ENST00000440875.5:c.703A>T	ENSP00000475553.2:p.Asn235Tyr
ENST00000497268.1:n.664A>T
ENST00000539609.7:c.646A>T	ENSP00000443792.2:p.Asn216Tyr
ENST00000558170.6:c.718A>T	ENSP00000454157.1:p.Asn240Tyr
ENST00000627532.2:c.718A>T	ENSP00000487174.1:p.Asn240Tyr
NM_001171653.1:c.646A>T	NP_001165124.1:p.Asn216Tyr
NM_014795.3:c.718A>T	NP_055610.1:p.Asn240Tyr
XM_006712881.2:c.718A>T	XP_006712944.1:p.Asn240Tyr
XM_006712882.2:c.718A>T	XP_006712945.1:p.Asn240Tyr
XM_011512231.1:c.709A>T	XP_011510533.1:p.Asn237Tyr
XM_011512232.1:c.697A>T	XP_011510534.1:p.Asn233Tyr
NM_014795.4:c.718A>T MANE Select	NP_055610.1:p.Asn240Tyr
NM_001171653.2:c.646A>T	NP_001165124.1:p.Asn216Tyr