Canonical Allele Identifier: CA429445222

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156837T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399270T>G , CM000664.2:g.144399270T>G	GRCh38
NC_000002.11:g.145156837T>G , CM000664.1:g.145156837T>G	GRCh37
NC_000002.10:g.144873307T>G	NCBI36
NG_016431.1:g.126122A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1766A>C	ENSP00000508434.1:n.*1766A>C
ENST00000440875.6:c.1140A>C	ENSP00000475553.3:p.Val380=
ENST00000627532.3:c.1917A>C MANE Select	ENSP00000487174.1:p.Val639=
ENST00000636026.2:c.1917A>C	ENSP00000490776.1:p.Val639=
ENST00000636179.1:n.1886A>C
ENST00000636413.1:c.1581A>C	ENSP00000490508.1:p.Val527=
ENST00000636471.1:c.1992A>C	ENSP00000490317.1:p.Val664=
ENST00000636732.2:c.*1634A>C	ENSP00000490175.1:n.*1634A>C
ENST00000636820.1:n.2017A>C
ENST00000637045.1:c.1581A>C	ENSP00000490141.1:p.Val527=
ENST00000637304.1:c.1581A>C	ENSP00000490872.1:p.Val527=
ENST00000638007.1:c.1581A>C	ENSP00000490723.1:p.Val527=
ENST00000638087.1:c.1581A>C	ENSP00000490673.1:p.Val527=
ENST00000638128.1:c.1140A>C	ENSP00000490934.1:p.Val380=
ENST00000675069.1:c.-133-420A>C	ENSP00000502467.1:n.-133-420A>C
ENST00000675145.1:n.2465A>C
ENST00000303660.8:c.1914A>C	ENSP00000302501.4:p.Val638=
ENST00000409487.7:c.1917A>C	ENSP00000386854.2:p.Val639=
ENST00000419938.5:c.655+1929A>C	ENSP00000394777.2:n.655+1929A>C
ENST00000427902.5:c.2004A>C	ENSP00000395496.2:p.Val668=
ENST00000440875.5:c.1167+267A>C	ENSP00000475553.2:n.1167+267A>C
ENST00000539609.7:c.1845A>C	ENSP00000443792.2:p.Val615=
ENST00000558170.6:c.1917A>C	ENSP00000454157.1:p.Val639=
ENST00000627532.2:c.1917A>C	ENSP00000487174.1:p.Val639=
NM_001171653.1:c.1845A>C	NP_001165124.1:p.Val615=
NM_014795.3:c.1917A>C	NP_055610.1:p.Val639=
XM_006712881.2:c.1917A>C	XP_006712944.1:p.Val639=
XM_006712882.2:c.1917A>C	XP_006712945.1:p.Val639=
XM_011512231.1:c.1908A>C	XP_011510533.1:p.Val636=
XM_011512232.1:c.1896A>C	XP_011510534.1:p.Val632=
NM_014795.4:c.1917A>C MANE Select	NP_055610.1:p.Val639=
NM_001171653.2:c.1845A>C	NP_001165124.1:p.Val615=