Canonical Allele Identifier: CA348714784

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161585C>G (hg19) ; chr2:g.144404018C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404018C>G , CM000664.2:g.144404018C>G	GRCh38
NC_000002.11:g.145161585C>G , CM000664.1:g.145161585C>G	GRCh37
NC_000002.10:g.144878055C>G	NCBI36
NG_016431.1:g.121374G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*554G>C	ENSP00000508434.1:n.*554G>C
ENST00000440875.6:c.-73G>C	ENSP00000475553.3:n.-73G>C
ENST00000627532.3:c.705G>C MANE Select	ENSP00000487174.1:p.Glu235Asp
ENST00000636026.2:c.705G>C	ENSP00000490776.1:p.Glu235Asp
ENST00000636179.1:n.674G>C
ENST00000636413.1:c.369G>C	ENSP00000490508.1:p.Glu123Asp
ENST00000636471.1:c.705G>C	ENSP00000490317.1:p.Glu235Asp
ENST00000636732.2:c.*422G>C	ENSP00000490175.1:n.*422G>C
ENST00000636820.1:n.805G>C
ENST00000637045.1:c.369G>C	ENSP00000490141.1:p.Glu123Asp
ENST00000637267.2:c.705G>C	ENSP00000490293.2:p.Glu235Asp
ENST00000637304.1:c.369G>C	ENSP00000490872.1:p.Glu123Asp
ENST00000638007.1:c.369G>C	ENSP00000490723.1:p.Glu123Asp
ENST00000638087.1:c.369G>C	ENSP00000490673.1:p.Glu123Asp
ENST00000638128.1:c.-73G>C	ENSP00000490934.1:n.-73G>C
ENST00000675069.1:c.-133-5168G>C	ENSP00000502467.1:n.-133-5168G>C
ENST00000303660.8:c.702G>C	ENSP00000302501.4:p.Glu234Asp
ENST00000392861.6:c.789G>C	ENSP00000376601.3:p.Glu263Asp
ENST00000409487.7:c.705G>C	ENSP00000386854.2:p.Glu235Asp
ENST00000419938.5:c.444G>C	ENSP00000394777.2:p.Glu148Asp
ENST00000427902.5:c.792G>C	ENSP00000395496.2:p.Glu264Asp
ENST00000440875.5:c.690G>C	ENSP00000475553.2:p.Glu230Asp
ENST00000497268.1:n.651G>C
ENST00000539609.7:c.633G>C	ENSP00000443792.2:p.Glu211Asp
ENST00000558170.6:c.705G>C	ENSP00000454157.1:p.Glu235Asp
ENST00000627532.2:c.705G>C	ENSP00000487174.1:p.Glu235Asp
NM_001171653.1:c.633G>C	NP_001165124.1:p.Glu211Asp
NM_014795.3:c.705G>C	NP_055610.1:p.Glu235Asp
XM_006712881.2:c.705G>C	XP_006712944.1:p.Glu235Asp
XM_006712882.2:c.705G>C	XP_006712945.1:p.Glu235Asp
XM_011512231.1:c.696G>C	XP_011510533.1:p.Glu232Asp
XM_011512232.1:c.684G>C	XP_011510534.1:p.Glu228Asp
NM_014795.4:c.705G>C MANE Select	NP_055610.1:p.Glu235Asp
NM_001171653.2:c.633G>C	NP_001165124.1:p.Glu211Asp