Canonical Allele Identifier: CA348709400

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156767A>G (hg19) ; chr2:g.144399200A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399200A>G , CM000664.2:g.144399200A>G	GRCh38
NC_000002.11:g.145156767A>G , CM000664.1:g.145156767A>G	GRCh37
NC_000002.10:g.144873237A>G	NCBI36
NG_016431.1:g.126192T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*1836T>C	ENSP00000508434.1:n.*1836T>C
ENST00000440875.6:c.1210T>C	ENSP00000475553.3:p.Tyr404His
ENST00000627532.3:c.1987T>C MANE Select	ENSP00000487174.1:p.Tyr663His
ENST00000636026.2:c.1987T>C	ENSP00000490776.1:p.Tyr663His
ENST00000636179.1:n.1956T>C
ENST00000636413.1:c.1651T>C	ENSP00000490508.1:p.Tyr551His
ENST00000636471.1:c.2062T>C	ENSP00000490317.1:p.Tyr688His
ENST00000636732.2:c.*1704T>C	ENSP00000490175.1:n.*1704T>C
ENST00000636820.1:n.2087T>C
ENST00000637045.1:c.1651T>C	ENSP00000490141.1:p.Tyr551His
ENST00000637304.1:c.1651T>C	ENSP00000490872.1:p.Tyr551His
ENST00000638007.1:c.1651T>C	ENSP00000490723.1:p.Tyr551His
ENST00000638087.1:c.1651T>C	ENSP00000490673.1:p.Tyr551His
ENST00000638128.1:c.1210T>C	ENSP00000490934.1:p.Tyr404His
ENST00000675069.1:c.-133-350T>C	ENSP00000502467.1:n.-133-350T>C
ENST00000675145.1:n.2535T>C
ENST00000303660.8:c.1984T>C	ENSP00000302501.4:p.Tyr662His
ENST00000409487.7:c.1987T>C	ENSP00000386854.2:p.Tyr663His
ENST00000419938.5:c.655+1999T>C	ENSP00000394777.2:n.655+1999T>C
ENST00000427902.5:c.2074T>C	ENSP00000395496.2:p.Tyr692His
ENST00000440875.5:c.1167+337T>C	ENSP00000475553.2:n.1167+337T>C
ENST00000539609.7:c.1915T>C	ENSP00000443792.2:p.Tyr639His
ENST00000558170.6:c.1987T>C	ENSP00000454157.1:p.Tyr663His
ENST00000627532.2:c.1987T>C	ENSP00000487174.1:p.Tyr663His
NM_001171653.1:c.1915T>C	NP_001165124.1:p.Tyr639His
NM_014795.3:c.1987T>C	NP_055610.1:p.Tyr663His
XM_006712881.2:c.1987T>C	XP_006712944.1:p.Tyr663His
XM_006712882.2:c.1987T>C	XP_006712945.1:p.Tyr663His
XM_011512231.1:c.1978T>C	XP_011510533.1:p.Tyr660His
XM_011512232.1:c.1966T>C	XP_011510534.1:p.Tyr656His
NM_014795.4:c.1987T>C MANE Select	NP_055610.1:p.Tyr663His
NM_001171653.2:c.1915T>C	NP_001165124.1:p.Tyr639His