Canonical Allele Identifier: CA348708413

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156371T>C (hg19) ; chr2:g.144398804T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398804T>C , CM000664.2:g.144398804T>C	GRCh38
NC_000002.11:g.145156371T>C , CM000664.1:g.145156371T>C	GRCh37
NC_000002.10:g.144872841T>C	NCBI36
NG_016431.1:g.126588A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2232A>G	ENSP00000508434.1:n.*2232A>G
ENST00000440875.6:c.1606A>G	ENSP00000475553.3:p.Asn536Asp
ENST00000627532.3:c.2383A>G MANE Select	ENSP00000487174.1:p.Asn795Asp
ENST00000636026.2:c.2383A>G	ENSP00000490776.1:p.Asn795Asp
ENST00000636179.1:n.2352A>G
ENST00000636413.1:c.2047A>G	ENSP00000490508.1:p.Asn683Asp
ENST00000636471.1:c.2458A>G	ENSP00000490317.1:p.Asn820Asp
ENST00000636732.2:c.*2100A>G	ENSP00000490175.1:n.*2100A>G
ENST00000636820.1:n.2483A>G
ENST00000637045.1:c.2047A>G	ENSP00000490141.1:p.Asn683Asp
ENST00000637304.1:c.2047A>G	ENSP00000490872.1:p.Asn683Asp
ENST00000638007.1:c.2047A>G	ENSP00000490723.1:p.Asn683Asp
ENST00000638087.1:c.2047A>G	ENSP00000490673.1:p.Asn683Asp
ENST00000638128.1:c.1606A>G	ENSP00000490934.1:p.Asn536Asp
ENST00000675069.1:c.-87A>G	ENSP00000502467.1:n.-87A>G
ENST00000675145.1:n.2931A>G
ENST00000303660.8:c.2380A>G	ENSP00000302501.4:p.Asn794Asp
ENST00000409487.7:c.2383A>G	ENSP00000386854.2:p.Asn795Asp
ENST00000419938.5:c.655+2395A>G	ENSP00000394777.2:n.655+2395A>G
ENST00000440875.5:c.1167+733A>G	ENSP00000475553.2:n.1167+733A>G
ENST00000539609.7:c.2311A>G	ENSP00000443792.2:p.Asn771Asp
ENST00000558170.6:c.2383A>G	ENSP00000454157.1:p.Asn795Asp
ENST00000627532.2:c.2383A>G	ENSP00000487174.1:p.Asn795Asp
NM_001171653.1:c.2311A>G	NP_001165124.1:p.Asn771Asp
NM_014795.3:c.2383A>G	NP_055610.1:p.Asn795Asp
XM_006712881.2:c.2383A>G	XP_006712944.1:p.Asn795Asp
XM_006712882.2:c.2383A>G	XP_006712945.1:p.Asn795Asp
XM_011512231.1:c.2374A>G	XP_011510533.1:p.Asn792Asp
XM_011512232.1:c.2362A>G	XP_011510534.1:p.Asn788Asp
NM_014795.4:c.2383A>G MANE Select	NP_055610.1:p.Asn795Asp
NM_001171653.2:c.2311A>G	NP_001165124.1:p.Asn771Asp