Canonical Allele Identifier: CA348699161

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147166T>A (hg19) ; chr2:g.144389599T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389599T>A , CM000664.2:g.144389599T>A	GRCh38
NC_000002.11:g.145147166T>A , CM000664.1:g.145147166T>A	GRCh37
NC_000002.10:g.144863636T>A	NCBI36
NG_016431.1:g.135793A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3346A>T	ENSP00000508434.1:n.*3346A>T
ENST00000440875.6:c.2720A>T	ENSP00000475553.3:p.Glu907Val
ENST00000627532.3:c.3497A>T MANE Select	ENSP00000487174.1:p.Glu1166Val
ENST00000636026.2:c.3385A>T	ENSP00000490776.1:p.Lys1129Ter
ENST00000636179.1:n.3466A>T
ENST00000636413.1:c.3161A>T	ENSP00000490508.1:p.Glu1054Val
ENST00000636471.1:c.3572A>T	ENSP00000490317.1:p.Glu1191Val
ENST00000636732.2:c.*3214A>T	ENSP00000490175.1:n.*3214A>T
ENST00000636820.1:n.3597A>T
ENST00000637045.1:c.3161A>T	ENSP00000490141.1:p.Glu1054Val
ENST00000637304.1:c.3161A>T	ENSP00000490872.1:p.Glu1054Val
ENST00000638007.1:c.3161A>T	ENSP00000490723.1:p.Glu1054Val
ENST00000638087.1:c.3161A>T	ENSP00000490673.1:p.Glu1054Val
ENST00000638128.1:c.2720A>T	ENSP00000490934.1:p.Glu907Val
ENST00000639389.1:c.151+6813A>T	ENSP00000492572.1:n.151+6813A>T
ENST00000647488.1:c.717A>T	ENSP00000494820.1:n.717A>T
ENST00000675069.1:c.1028A>T	ENSP00000502467.1:p.Glu343Val
ENST00000303660.8:c.3494A>T	ENSP00000302501.4:p.Glu1165Val
ENST00000409487.7:c.3497A>T	ENSP00000386854.2:p.Glu1166Val
ENST00000419938.5:c.656-717A>T	ENSP00000394777.2:n.656-717A>T
ENST00000539609.7:c.3425A>T	ENSP00000443792.2:p.Glu1142Val
ENST00000558170.6:c.3497A>T	ENSP00000454157.1:p.Glu1166Val
ENST00000627532.2:c.3497A>T	ENSP00000487174.1:p.Glu1166Val
NM_001171653.1:c.3425A>T	NP_001165124.1:p.Glu1142Val
NM_014795.3:c.3497A>T	NP_055610.1:p.Glu1166Val
XM_006712881.2:c.3497A>T	XP_006712944.1:p.Glu1166Val
XM_006712882.2:c.3497A>T	XP_006712945.1:p.Glu1166Val
XM_011512231.1:c.3488A>T	XP_011510533.1:p.Glu1163Val
XM_011512232.1:c.3476A>T	XP_011510534.1:p.Glu1159Val
NM_014795.4:c.3497A>T MANE Select	NP_055610.1:p.Glu1166Val
NM_001171653.2:c.3425A>T	NP_001165124.1:p.Glu1142Val