Canonical Allele Identifier: CA2577114248

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144403847-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403847C>T , CM000664.2:g.144403847C>T	GRCh38
NC_000002.11:g.145161414C>T , CM000664.1:g.145161414C>T	GRCh37
NC_000002.10:g.144877884C>T	NCBI36
NG_016431.1:g.121545G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*656+69G>A	ENSP00000508434.1:n.*656+69G>A
ENST00000440875.6:c.30+69G>A	ENSP00000475553.3:n.30+69G>A
ENST00000627532.3:c.807+69G>A MANE Select	ENSP00000487174.1:n.807+69G>A
ENST00000636026.2:c.807+69G>A	ENSP00000490776.1:n.807+69G>A
ENST00000636179.1:n.776+69G>A
ENST00000636413.1:c.471+69G>A	ENSP00000490508.1:n.471+69G>A
ENST00000636471.1:c.807+69G>A	ENSP00000490317.1:n.807+69G>A
ENST00000636732.2:c.*524+69G>A	ENSP00000490175.1:n.*524+69G>A
ENST00000636820.1:n.907+69G>A
ENST00000637045.1:c.471+69G>A	ENSP00000490141.1:n.471+69G>A
ENST00000637267.2:c.807+69G>A	ENSP00000490293.2:n.807+69G>A
ENST00000637304.1:c.471+69G>A	ENSP00000490872.1:n.471+69G>A
ENST00000638007.1:c.471+69G>A	ENSP00000490723.1:n.471+69G>A
ENST00000638087.1:c.471+69G>A	ENSP00000490673.1:n.471+69G>A
ENST00000638128.1:c.30+69G>A	ENSP00000490934.1:n.30+69G>A
ENST00000675069.1:c.-133-4997G>A	ENSP00000502467.1:n.-133-4997G>A
ENST00000303660.8:c.804+69G>A	ENSP00000302501.4:n.804+69G>A
ENST00000392861.6:c.891+69G>A	ENSP00000376601.3:n.891+69G>A
ENST00000409487.7:c.807+69G>A	ENSP00000386854.2:n.807+69G>A
ENST00000419938.5:c.546+69G>A	ENSP00000394777.2:n.546+69G>A
ENST00000427902.5:c.894+69G>A	ENSP00000395496.2:n.894+69G>A
ENST00000440875.5:c.792+69G>A	ENSP00000475553.2:n.792+69G>A
ENST00000539609.7:c.735+69G>A	ENSP00000443792.2:n.735+69G>A
ENST00000558170.6:c.807+69G>A	ENSP00000454157.1:n.807+69G>A
ENST00000627532.2:c.807+69G>A	ENSP00000487174.1:n.807+69G>A
NM_001171653.1:c.735+69G>A	NP_001165124.1:n.735+69G>A
NM_014795.3:c.807+69G>A	NP_055610.1:n.807+69G>A
XM_006712881.2:c.807+69G>A	XP_006712944.1:n.807+69G>A
XM_006712882.2:c.807+69G>A	XP_006712945.1:n.807+69G>A
XM_011512231.1:c.798+69G>A	XP_011510533.1:n.798+69G>A
XM_011512232.1:c.786+69G>A	XP_011510534.1:n.786+69G>A
NM_014795.4:c.807+69G>A MANE Select	NP_055610.1:n.807+69G>A
NM_001171653.2:c.735+69G>A	NP_001165124.1:n.735+69G>A