Canonical Allele Identifier: CA429441122

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 794862
• ClinVar RCV Id: RCV001408323
• dbSNP Id: rs1573707737
• MyVariant Identifiers: chr2:g.145147204T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389637T>C , CM000664.2:g.144389637T>C	GRCh38
NC_000002.11:g.145147204T>C , CM000664.1:g.145147204T>C	GRCh37
NC_000002.10:g.144863674T>C	NCBI36
NG_016431.1:g.135755A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3308A>G	ENSP00000508434.1:n.*3308A>G
ENST00000440875.6:c.2682A>G	ENSP00000475553.3:p.Arg894=
ENST00000627532.3:c.3459A>G MANE Select	ENSP00000487174.1:p.Arg1153=
ENST00000636026.2:c.3347A>G	ENSP00000490776.1:p.Asp1116Gly
ENST00000636179.1:n.3428A>G
ENST00000636413.1:c.3123A>G	ENSP00000490508.1:p.Arg1041=
ENST00000636471.1:c.3534A>G	ENSP00000490317.1:p.Arg1178=
ENST00000636732.2:c.*3176A>G	ENSP00000490175.1:n.*3176A>G
ENST00000636820.1:n.3559A>G
ENST00000637045.1:c.3123A>G	ENSP00000490141.1:p.Arg1041=
ENST00000637304.1:c.3123A>G	ENSP00000490872.1:p.Arg1041=
ENST00000638007.1:c.3123A>G	ENSP00000490723.1:p.Arg1041=
ENST00000638087.1:c.3123A>G	ENSP00000490673.1:p.Arg1041=
ENST00000638128.1:c.2682A>G	ENSP00000490934.1:p.Arg894=
ENST00000639389.1:c.151+6775A>G	ENSP00000492572.1:n.151+6775A>G
ENST00000647488.1:c.679A>G	ENSP00000494820.1:n.679A>G
ENST00000675069.1:c.990A>G	ENSP00000502467.1:p.Arg330=
ENST00000303660.8:c.3456A>G	ENSP00000302501.4:p.Arg1152=
ENST00000409487.7:c.3459A>G	ENSP00000386854.2:p.Arg1153=
ENST00000419938.5:c.656-755A>G	ENSP00000394777.2:n.656-755A>G
ENST00000539609.7:c.3387A>G	ENSP00000443792.2:p.Arg1129=
ENST00000558170.6:c.3459A>G	ENSP00000454157.1:p.Arg1153=
ENST00000627532.2:c.3459A>G	ENSP00000487174.1:p.Arg1153=
NM_001171653.1:c.3387A>G	NP_001165124.1:p.Arg1129=
NM_014795.3:c.3459A>G	NP_055610.1:p.Arg1153=
XM_006712881.2:c.3459A>G	XP_006712944.1:p.Arg1153=
XM_006712882.2:c.3459A>G	XP_006712945.1:p.Arg1153=
XM_011512231.1:c.3450A>G	XP_011510533.1:p.Arg1150=
XM_011512232.1:c.3438A>G	XP_011510534.1:p.Arg1146=
NM_014795.4:c.3459A>G MANE Select	NP_055610.1:p.Arg1153=
NM_001171653.2:c.3387A>G	NP_001165124.1:p.Arg1129=