Canonical Allele Identifier: CA348714861

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161619G>C (hg19) ; chr2:g.144404052G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404052G>C , CM000664.2:g.144404052G>C	GRCh38
NC_000002.11:g.145161619G>C , CM000664.1:g.145161619G>C	GRCh37
NC_000002.10:g.144878089G>C	NCBI36
NG_016431.1:g.121340C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*520C>G	ENSP00000508434.1:n.*520C>G
ENST00000440875.6:c.-107C>G	ENSP00000475553.3:n.-107C>G
ENST00000627532.3:c.671C>G MANE Select	ENSP00000487174.1:p.Thr224Arg
ENST00000636026.2:c.671C>G	ENSP00000490776.1:p.Thr224Arg
ENST00000636179.1:n.640C>G
ENST00000636413.1:c.335C>G	ENSP00000490508.1:p.Thr112Arg
ENST00000636471.1:c.671C>G	ENSP00000490317.1:p.Thr224Arg
ENST00000636732.2:c.*388C>G	ENSP00000490175.1:n.*388C>G
ENST00000636820.1:n.771C>G
ENST00000637045.1:c.335C>G	ENSP00000490141.1:p.Thr112Arg
ENST00000637267.2:c.671C>G	ENSP00000490293.2:p.Thr224Arg
ENST00000637304.1:c.335C>G	ENSP00000490872.1:p.Thr112Arg
ENST00000638007.1:c.335C>G	ENSP00000490723.1:p.Thr112Arg
ENST00000638087.1:c.335C>G	ENSP00000490673.1:p.Thr112Arg
ENST00000638128.1:c.-107C>G	ENSP00000490934.1:n.-107C>G
ENST00000675069.1:c.-133-5202C>G	ENSP00000502467.1:n.-133-5202C>G
ENST00000303660.8:c.668C>G	ENSP00000302501.4:p.Thr223Arg
ENST00000392861.6:c.755C>G	ENSP00000376601.3:p.Thr252Arg
ENST00000409487.7:c.671C>G	ENSP00000386854.2:p.Thr224Arg
ENST00000419938.5:c.410C>G	ENSP00000394777.2:p.Thr137Arg
ENST00000427902.5:c.758C>G	ENSP00000395496.2:p.Thr253Arg
ENST00000440875.5:c.656C>G	ENSP00000475553.2:p.Thr219Arg
ENST00000497268.1:n.617C>G
ENST00000539609.7:c.599C>G	ENSP00000443792.2:p.Thr200Arg
ENST00000558170.6:c.671C>G	ENSP00000454157.1:p.Thr224Arg
ENST00000627532.2:c.671C>G	ENSP00000487174.1:p.Thr224Arg
NM_001171653.1:c.599C>G	NP_001165124.1:p.Thr200Arg
NM_014795.3:c.671C>G	NP_055610.1:p.Thr224Arg
XM_006712881.2:c.671C>G	XP_006712944.1:p.Thr224Arg
XM_006712882.2:c.671C>G	XP_006712945.1:p.Thr224Arg
XM_011512231.1:c.662C>G	XP_011510533.1:p.Thr221Arg
XM_011512232.1:c.650C>G	XP_011510534.1:p.Thr217Arg
NM_014795.4:c.671C>G MANE Select	NP_055610.1:p.Thr224Arg
NM_001171653.2:c.599C>G	NP_001165124.1:p.Thr200Arg