Canonical Allele Identifier: CA348699938

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147398C>G (hg19) ; chr2:g.144389831C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389831C>G , CM000664.2:g.144389831C>G	GRCh38
NC_000002.11:g.145147398C>G , CM000664.1:g.145147398C>G	GRCh37
NC_000002.10:g.144863868C>G	NCBI36
NG_016431.1:g.135561G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3114G>C	ENSP00000508434.1:n.*3114G>C
ENST00000440875.6:c.2488G>C	ENSP00000475553.3:p.Glu830Gln
ENST00000627532.3:c.3265G>C MANE Select	ENSP00000487174.1:p.Glu1089Gln
ENST00000636026.2:c.3230+35G>C	ENSP00000490776.1:n.3230+35G>C
ENST00000636179.1:n.3234G>C
ENST00000636413.1:c.2929G>C	ENSP00000490508.1:p.Glu977Gln
ENST00000636471.1:c.3340G>C	ENSP00000490317.1:p.Glu1114Gln
ENST00000636732.2:c.*2982G>C	ENSP00000490175.1:n.*2982G>C
ENST00000636820.1:n.3365G>C
ENST00000637045.1:c.2929G>C	ENSP00000490141.1:p.Glu977Gln
ENST00000637304.1:c.2929G>C	ENSP00000490872.1:p.Glu977Gln
ENST00000638007.1:c.2929G>C	ENSP00000490723.1:p.Glu977Gln
ENST00000638087.1:c.2929G>C	ENSP00000490673.1:p.Glu977Gln
ENST00000638128.1:c.2488G>C	ENSP00000490934.1:p.Glu830Gln
ENST00000639389.1:c.151+6581G>C	ENSP00000492572.1:n.151+6581G>C
ENST00000647488.1:c.485G>C	ENSP00000494820.1:n.485G>C
ENST00000675069.1:c.796G>C	ENSP00000502467.1:p.Glu266Gln
ENST00000303660.8:c.3262G>C	ENSP00000302501.4:p.Glu1088Gln
ENST00000409487.7:c.3265G>C	ENSP00000386854.2:p.Glu1089Gln
ENST00000419938.5:c.656-949G>C	ENSP00000394777.2:n.656-949G>C
ENST00000539609.7:c.3193G>C	ENSP00000443792.2:p.Glu1065Gln
ENST00000558170.6:c.3265G>C	ENSP00000454157.1:p.Glu1089Gln
ENST00000627532.2:c.3265G>C	ENSP00000487174.1:p.Glu1089Gln
NM_001171653.1:c.3193G>C	NP_001165124.1:p.Glu1065Gln
NM_014795.3:c.3265G>C	NP_055610.1:p.Glu1089Gln
XM_006712881.2:c.3265G>C	XP_006712944.1:p.Glu1089Gln
XM_006712882.2:c.3265G>C	XP_006712945.1:p.Glu1089Gln
XM_011512231.1:c.3256G>C	XP_011510533.1:p.Glu1086Gln
XM_011512232.1:c.3244G>C	XP_011510534.1:p.Glu1082Gln
NM_014795.4:c.3265G>C MANE Select	NP_055610.1:p.Glu1089Gln
NM_001171653.2:c.3193G>C	NP_001165124.1:p.Glu1065Gln