Canonical Allele Identifier: CA2661360180

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144403834-TTAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403839_144403841del , CM000664.2:g.144403839_144403841del	GRCh38
NC_000002.11:g.145161406_145161408del , CM000664.1:g.145161406_145161408del	GRCh37
NC_000002.10:g.144877876_144877878del	NCBI36
NG_016431.1:g.121555_121557del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*656+79_*656+81del	ENSP00000508434.1:n.*656+79_*656+81del
ENST00000440875.6:c.30+79_30+81del	ENSP00000475553.3:n.30+79_30+81del
ENST00000627532.3:c.807+79_807+81del MANE Select	ENSP00000487174.1:n.807+79_807+81del
ENST00000636026.2:c.807+79_807+81del	ENSP00000490776.1:n.807+79_807+81del
ENST00000636179.1:n.776+79_776+81del
ENST00000636413.1:c.471+79_471+81del	ENSP00000490508.1:n.471+79_471+81del
ENST00000636471.1:c.807+79_807+81del	ENSP00000490317.1:n.807+79_807+81del
ENST00000636732.2:c.*524+79_*524+81del	ENSP00000490175.1:n.*524+79_*524+81del
ENST00000636820.1:n.907+79_907+81del
ENST00000637045.1:c.471+79_471+81del	ENSP00000490141.1:n.471+79_471+81del
ENST00000637267.2:c.807+79_807+81del	ENSP00000490293.2:n.807+79_807+81del
ENST00000637304.1:c.471+79_471+81del	ENSP00000490872.1:n.471+79_471+81del
ENST00000638007.1:c.471+79_471+81del	ENSP00000490723.1:n.471+79_471+81del
ENST00000638087.1:c.471+79_471+81del	ENSP00000490673.1:n.471+79_471+81del
ENST00000638128.1:c.30+79_30+81del	ENSP00000490934.1:n.30+79_30+81del
ENST00000675069.1:c.-133-4987_-133-4985del	ENSP00000502467.1:n.-133-4987_-133-4985del
ENST00000303660.8:c.804+79_804+81del	ENSP00000302501.4:n.804+79_804+81del
ENST00000392861.6:c.891+79_891+81del	ENSP00000376601.3:n.891+79_891+81del
ENST00000409487.7:c.807+79_807+81del	ENSP00000386854.2:n.807+79_807+81del
ENST00000419938.5:c.546+79_546+81del	ENSP00000394777.2:n.546+79_546+81del
ENST00000427902.5:c.894+79_894+81del	ENSP00000395496.2:n.894+79_894+81del
ENST00000440875.5:c.792+79_792+81del	ENSP00000475553.2:n.792+79_792+81del
ENST00000539609.7:c.735+79_735+81del	ENSP00000443792.2:n.735+79_735+81del
ENST00000558170.6:c.807+79_807+81del	ENSP00000454157.1:n.807+79_807+81del
ENST00000627532.2:c.807+79_807+81del	ENSP00000487174.1:n.807+79_807+81del
NM_001171653.1:c.735+79_735+81del	NP_001165124.1:n.735+79_735+81del
NM_014795.3:c.807+79_807+81del	NP_055610.1:n.807+79_807+81del
XM_006712881.2:c.807+79_807+81del	XP_006712944.1:n.807+79_807+81del
XM_006712882.2:c.807+79_807+81del	XP_006712945.1:n.807+79_807+81del
XM_011512231.1:c.798+79_798+81del	XP_011510533.1:n.798+79_798+81del
XM_011512232.1:c.786+79_786+81del	XP_011510534.1:n.786+79_786+81del
NM_014795.4:c.807+79_807+81del MANE Select	NP_055610.1:n.807+79_807+81del
NM_001171653.2:c.735+79_735+81del	NP_001165124.1:n.735+79_735+81del