Canonical Allele Identifier: CA348708281

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156314C>G (hg19) ; chr2:g.144398747C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398747C>G , CM000664.2:g.144398747C>G	GRCh38
NC_000002.11:g.145156314C>G , CM000664.1:g.145156314C>G	GRCh37
NC_000002.10:g.144872784C>G	NCBI36
NG_016431.1:g.126645G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2289G>C	ENSP00000508434.1:n.*2289G>C
ENST00000440875.6:c.1663G>C	ENSP00000475553.3:p.Glu555Gln
ENST00000627532.3:c.2440G>C MANE Select	ENSP00000487174.1:p.Glu814Gln
ENST00000636026.2:c.2440G>C	ENSP00000490776.1:p.Glu814Gln
ENST00000636179.1:n.2409G>C
ENST00000636413.1:c.2104G>C	ENSP00000490508.1:p.Glu702Gln
ENST00000636471.1:c.2515G>C	ENSP00000490317.1:p.Glu839Gln
ENST00000636732.2:c.*2157G>C	ENSP00000490175.1:n.*2157G>C
ENST00000636820.1:n.2540G>C
ENST00000637045.1:c.2104G>C	ENSP00000490141.1:p.Glu702Gln
ENST00000637304.1:c.2104G>C	ENSP00000490872.1:p.Glu702Gln
ENST00000638007.1:c.2104G>C	ENSP00000490723.1:p.Glu702Gln
ENST00000638087.1:c.2104G>C	ENSP00000490673.1:p.Glu702Gln
ENST00000638128.1:c.1663G>C	ENSP00000490934.1:p.Glu555Gln
ENST00000675069.1:c.-30G>C	ENSP00000502467.1:n.-30G>C
ENST00000675145.1:n.2988G>C
ENST00000303660.8:c.2437G>C	ENSP00000302501.4:p.Glu813Gln
ENST00000409487.7:c.2440G>C	ENSP00000386854.2:p.Glu814Gln
ENST00000419938.5:c.655+2452G>C	ENSP00000394777.2:n.655+2452G>C
ENST00000440875.5:c.1167+790G>C	ENSP00000475553.2:n.1167+790G>C
ENST00000539609.7:c.2368G>C	ENSP00000443792.2:p.Glu790Gln
ENST00000558170.6:c.2440G>C	ENSP00000454157.1:p.Glu814Gln
ENST00000627532.2:c.2440G>C	ENSP00000487174.1:p.Glu814Gln
NM_001171653.1:c.2368G>C	NP_001165124.1:p.Glu790Gln
NM_014795.3:c.2440G>C	NP_055610.1:p.Glu814Gln
XM_006712881.2:c.2440G>C	XP_006712944.1:p.Glu814Gln
XM_006712882.2:c.2440G>C	XP_006712945.1:p.Glu814Gln
XM_011512231.1:c.2431G>C	XP_011510533.1:p.Glu811Gln
XM_011512232.1:c.2419G>C	XP_011510534.1:p.Glu807Gln
NM_014795.4:c.2440G>C MANE Select	NP_055610.1:p.Glu814Gln
NM_001171653.2:c.2368G>C	NP_001165124.1:p.Glu790Gln