Canonical Allele Identifier: CA429445298

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156294T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398727T>C , CM000664.2:g.144398727T>C	GRCh38
NC_000002.11:g.145156294T>C , CM000664.1:g.145156294T>C	GRCh37
NC_000002.10:g.144872764T>C	NCBI36
NG_016431.1:g.126665A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2309A>G	ENSP00000508434.1:n.*2309A>G
ENST00000440875.6:c.1683A>G	ENSP00000475553.3:p.Leu561=
ENST00000627532.3:c.2460A>G MANE Select	ENSP00000487174.1:p.Leu820=
ENST00000636026.2:c.2460A>G	ENSP00000490776.1:p.Leu820=
ENST00000636179.1:n.2429A>G
ENST00000636413.1:c.2124A>G	ENSP00000490508.1:p.Leu708=
ENST00000636471.1:c.2535A>G	ENSP00000490317.1:p.Leu845=
ENST00000636732.2:c.*2177A>G	ENSP00000490175.1:n.*2177A>G
ENST00000636820.1:n.2560A>G
ENST00000637045.1:c.2124A>G	ENSP00000490141.1:p.Leu708=
ENST00000637304.1:c.2124A>G	ENSP00000490872.1:p.Leu708=
ENST00000638007.1:c.2124A>G	ENSP00000490723.1:p.Leu708=
ENST00000638087.1:c.2124A>G	ENSP00000490673.1:p.Leu708=
ENST00000638128.1:c.1683A>G	ENSP00000490934.1:p.Leu561=
ENST00000675069.1:c.-10A>G	ENSP00000502467.1:n.-10A>G
ENST00000675145.1:n.3008A>G
ENST00000303660.8:c.2457A>G	ENSP00000302501.4:p.Leu819=
ENST00000409487.7:c.2460A>G	ENSP00000386854.2:p.Leu820=
ENST00000419938.5:c.655+2472A>G	ENSP00000394777.2:n.655+2472A>G
ENST00000440875.5:c.1168-799A>G	ENSP00000475553.2:n.1168-799A>G
ENST00000539609.7:c.2388A>G	ENSP00000443792.2:p.Leu796=
ENST00000558170.6:c.2460A>G	ENSP00000454157.1:p.Leu820=
ENST00000627532.2:c.2460A>G	ENSP00000487174.1:p.Leu820=
NM_001171653.1:c.2388A>G	NP_001165124.1:p.Leu796=
NM_014795.3:c.2460A>G	NP_055610.1:p.Leu820=
XM_006712881.2:c.2460A>G	XP_006712944.1:p.Leu820=
XM_006712882.2:c.2460A>G	XP_006712945.1:p.Leu820=
XM_011512231.1:c.2451A>G	XP_011510533.1:p.Leu817=
XM_011512232.1:c.2439A>G	XP_011510534.1:p.Leu813=
NM_014795.4:c.2460A>G MANE Select	NP_055610.1:p.Leu820=
NM_001171653.2:c.2388A>G	NP_001165124.1:p.Leu796=