Canonical Allele Identifier: CA429445867

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144399204-T-C
• MyVariant Identifiers: chr2:g.145156771T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399204T>C , CM000664.2:g.144399204T>C	GRCh38
NC_000002.11:g.145156771T>C , CM000664.1:g.145156771T>C	GRCh37
NC_000002.10:g.144873241T>C	NCBI36
NG_016431.1:g.126188A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*1832A>G	ENSP00000508434.1:n.*1832A>G
ENST00000440875.6:c.1206A>G	ENSP00000475553.3:p.Ala402=
ENST00000627532.3:c.1983A>G MANE Select	ENSP00000487174.1:p.Ala661=
ENST00000636026.2:c.1983A>G	ENSP00000490776.1:p.Ala661=
ENST00000636179.1:n.1952A>G
ENST00000636413.1:c.1647A>G	ENSP00000490508.1:p.Ala549=
ENST00000636471.1:c.2058A>G	ENSP00000490317.1:p.Ala686=
ENST00000636732.2:c.*1700A>G	ENSP00000490175.1:n.*1700A>G
ENST00000636820.1:n.2083A>G
ENST00000637045.1:c.1647A>G	ENSP00000490141.1:p.Ala549=
ENST00000637304.1:c.1647A>G	ENSP00000490872.1:p.Ala549=
ENST00000638007.1:c.1647A>G	ENSP00000490723.1:p.Ala549=
ENST00000638087.1:c.1647A>G	ENSP00000490673.1:p.Ala549=
ENST00000638128.1:c.1206A>G	ENSP00000490934.1:p.Ala402=
ENST00000675069.1:c.-133-354A>G	ENSP00000502467.1:n.-133-354A>G
ENST00000675145.1:n.2531A>G
ENST00000303660.8:c.1980A>G	ENSP00000302501.4:p.Ala660=
ENST00000409487.7:c.1983A>G	ENSP00000386854.2:p.Ala661=
ENST00000419938.5:c.655+1995A>G	ENSP00000394777.2:n.655+1995A>G
ENST00000427902.5:c.2070A>G	ENSP00000395496.2:p.Ala690=
ENST00000440875.5:c.1167+333A>G	ENSP00000475553.2:n.1167+333A>G
ENST00000539609.7:c.1911A>G	ENSP00000443792.2:p.Ala637=
ENST00000558170.6:c.1983A>G	ENSP00000454157.1:p.Ala661=
ENST00000627532.2:c.1983A>G	ENSP00000487174.1:p.Ala661=
NM_001171653.1:c.1911A>G	NP_001165124.1:p.Ala637=
NM_014795.3:c.1983A>G	NP_055610.1:p.Ala661=
XM_006712881.2:c.1983A>G	XP_006712944.1:p.Ala661=
XM_006712882.2:c.1983A>G	XP_006712945.1:p.Ala661=
XM_011512231.1:c.1974A>G	XP_011510533.1:p.Ala658=
XM_011512232.1:c.1962A>G	XP_011510534.1:p.Ala654=
NM_014795.4:c.1983A>G MANE Select	NP_055610.1:p.Ala661=
NM_001171653.2:c.1911A>G	NP_001165124.1:p.Ala637=