Canonical Allele Identifier: CA645521248

Gene: ZEB2

Linked Data

• COSMIC: COSM1716907

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399313dup , CM000664.2:g.144399313dup	GRCh38
NC_000002.11:g.145156880dup , CM000664.1:g.145156880dup	GRCh37
NC_000002.10:g.144873350dup	NCBI36
NG_016431.1:g.126080dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1724dup	ENSP00000508434.1:n.*1724dup
ENST00000440875.6:c.1098dup	ENSP00000475553.3:p.Gly367ArgfsTer5
ENST00000627532.3:c.1875dup MANE Select	ENSP00000487174.1:p.Gly626ArgfsTer5
ENST00000636026.2:c.1875dup	ENSP00000490776.1:p.Gly626ArgfsTer5
ENST00000636179.1:n.1844dup
ENST00000636413.1:c.1539dup	ENSP00000490508.1:p.Gly514ArgfsTer5
ENST00000636471.1:c.1950dup	ENSP00000490317.1:p.Gly651ArgfsTer5
ENST00000636732.2:c.*1592dup	ENSP00000490175.1:n.*1592dup
ENST00000636820.1:n.1975dup
ENST00000637045.1:c.1539dup	ENSP00000490141.1:p.Gly514ArgfsTer5
ENST00000637304.1:c.1539dup	ENSP00000490872.1:p.Gly514ArgfsTer5
ENST00000638007.1:c.1539dup	ENSP00000490723.1:p.Gly514ArgfsTer5
ENST00000638087.1:c.1539dup	ENSP00000490673.1:p.Gly514ArgfsTer5
ENST00000638128.1:c.1098dup	ENSP00000490934.1:p.Gly367ArgfsTer5
ENST00000675069.1:c.-133-462dup	ENSP00000502467.1:n.-133-462dup
ENST00000675145.1:n.2423dup
ENST00000303660.8:c.1872dup	ENSP00000302501.4:p.Gly625ArgfsTer5
ENST00000409487.7:c.1875dup	ENSP00000386854.2:p.Gly626ArgfsTer5
ENST00000419938.5:c.655+1887dup	ENSP00000394777.2:n.655+1887dup
ENST00000427902.5:c.1962dup	ENSP00000395496.2:p.Gly655ArgfsTer5
ENST00000440875.5:c.1167+225dup	ENSP00000475553.2:n.1167+225dup
ENST00000539609.7:c.1803dup	ENSP00000443792.2:p.Gly602ArgfsTer5
ENST00000558170.6:c.1875dup	ENSP00000454157.1:p.Gly626ArgfsTer5
ENST00000627532.2:c.1875dup	ENSP00000487174.1:p.Gly626ArgfsTer5
NM_001171653.1:c.1803dup	NP_001165124.1:p.Gly602ArgfsTer5
NM_014795.3:c.1875dup	NP_055610.1:p.Gly626ArgfsTer5
XM_006712881.2:c.1875dup	XP_006712944.1:p.Gly626ArgfsTer5
XM_006712882.2:c.1875dup	XP_006712945.1:p.Gly626ArgfsTer5
XM_011512231.1:c.1866dup	XP_011510533.1:p.Gly623ArgfsTer5
XM_011512232.1:c.1854dup	XP_011510534.1:p.Gly619ArgfsTer5
NM_014795.4:c.1875dup MANE Select	NP_055610.1:p.Gly626ArgfsTer5
NM_001171653.2:c.1803dup	NP_001165124.1:p.Gly602ArgfsTer5