Canonical Allele Identifier: CA348700006

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147411C>G (hg19) ; chr2:g.144389844C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389844C>G , CM000664.2:g.144389844C>G	GRCh38
NC_000002.11:g.145147411C>G , CM000664.1:g.145147411C>G	GRCh37
NC_000002.10:g.144863881C>G	NCBI36
NG_016431.1:g.135548G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3101G>C	ENSP00000508434.1:n.*3101G>C
ENST00000440875.6:c.2475G>C	ENSP00000475553.3:p.Glu825Asp
ENST00000627532.3:c.3252G>C MANE Select	ENSP00000487174.1:p.Glu1084Asp
ENST00000636026.2:c.3230+22G>C	ENSP00000490776.1:n.3230+22G>C
ENST00000636179.1:n.3221G>C
ENST00000636413.1:c.2916G>C	ENSP00000490508.1:p.Glu972Asp
ENST00000636471.1:c.3327G>C	ENSP00000490317.1:p.Glu1109Asp
ENST00000636732.2:c.*2969G>C	ENSP00000490175.1:n.*2969G>C
ENST00000636820.1:n.3352G>C
ENST00000637045.1:c.2916G>C	ENSP00000490141.1:p.Glu972Asp
ENST00000637304.1:c.2916G>C	ENSP00000490872.1:p.Glu972Asp
ENST00000638007.1:c.2916G>C	ENSP00000490723.1:p.Glu972Asp
ENST00000638087.1:c.2916G>C	ENSP00000490673.1:p.Glu972Asp
ENST00000638128.1:c.2475G>C	ENSP00000490934.1:p.Glu825Asp
ENST00000639389.1:c.151+6568G>C	ENSP00000492572.1:n.151+6568G>C
ENST00000647488.1:c.472G>C	ENSP00000494820.1:n.472G>C
ENST00000675069.1:c.783G>C	ENSP00000502467.1:p.Glu261Asp
ENST00000303660.8:c.3249G>C	ENSP00000302501.4:p.Glu1083Asp
ENST00000409487.7:c.3252G>C	ENSP00000386854.2:p.Glu1084Asp
ENST00000419938.5:c.656-962G>C	ENSP00000394777.2:n.656-962G>C
ENST00000539609.7:c.3180G>C	ENSP00000443792.2:p.Glu1060Asp
ENST00000558170.6:c.3252G>C	ENSP00000454157.1:p.Glu1084Asp
ENST00000627532.2:c.3252G>C	ENSP00000487174.1:p.Glu1084Asp
NM_001171653.1:c.3180G>C	NP_001165124.1:p.Glu1060Asp
NM_014795.3:c.3252G>C	NP_055610.1:p.Glu1084Asp
XM_006712881.2:c.3252G>C	XP_006712944.1:p.Glu1084Asp
XM_006712882.2:c.3252G>C	XP_006712945.1:p.Glu1084Asp
XM_011512231.1:c.3243G>C	XP_011510533.1:p.Glu1081Asp
XM_011512232.1:c.3231G>C	XP_011510534.1:p.Glu1077Asp
NM_014795.4:c.3252G>C MANE Select	NP_055610.1:p.Glu1084Asp
NM_001171653.2:c.3180G>C	NP_001165124.1:p.Glu1060Asp