Canonical Allele Identifier: CA645521251

Gene: ZEB2

Linked Data

• COSMIC: COSM5627652

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399717_144399718insGATA , CM000664.2:g.144399717_144399718insGATA	GRCh38
NC_000002.11:g.145157284_145157285insGATA , CM000664.1:g.145157284_145157285insGATA	GRCh37
NC_000002.10:g.144873754_144873755insGATA	NCBI36
NG_016431.1:g.125674_125675insTATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1318_*1319insTATC	ENSP00000508434.1:n.*1318_*1319insTATC
ENST00000440875.6:c.692_693insTATC	ENSP00000475553.3:p.Met232IlefsTer10
ENST00000627532.3:c.1469_1470insTATC MANE Select	ENSP00000487174.1:p.Met491IlefsTer10
ENST00000636026.2:c.1469_1470insTATC	ENSP00000490776.1:p.Met491IlefsTer10
ENST00000636179.1:n.1438_1439insTATC
ENST00000636413.1:c.1133_1134insTATC	ENSP00000490508.1:p.Met379IlefsTer10
ENST00000636471.1:c.1544_1545insTATC	ENSP00000490317.1:p.Met516IlefsTer10
ENST00000636732.2:c.*1186_*1187insTATC	ENSP00000490175.1:n.*1186_*1187insTATC
ENST00000636820.1:n.1569_1570insTATC
ENST00000637045.1:c.1133_1134insTATC	ENSP00000490141.1:p.Met379IlefsTer10
ENST00000637267.2:c.1469_1470insTATC	ENSP00000490293.2:p.Met491IlefsTer10
ENST00000637304.1:c.1133_1134insTATC	ENSP00000490872.1:p.Met379IlefsTer10
ENST00000638007.1:c.1133_1134insTATC	ENSP00000490723.1:p.Met379IlefsTer10
ENST00000638087.1:c.1133_1134insTATC	ENSP00000490673.1:p.Met379IlefsTer10
ENST00000638128.1:c.692_693insTATC	ENSP00000490934.1:p.Met232IlefsTer10
ENST00000675069.1:c.-133-868_-133-867insTATC	ENSP00000502467.1:n.-133-868_-133-867insTATC
ENST00000675145.1:n.2017_2018insTATC
ENST00000303660.8:c.1466_1467insTATC	ENSP00000302501.4:p.Met490IlefsTer10
ENST00000409487.7:c.1469_1470insTATC	ENSP00000386854.2:p.Met491IlefsTer10
ENST00000419938.5:c.655+1481_655+1482insTATC	ENSP00000394777.2:n.655+1481_655+1482insTATC
ENST00000427902.5:c.1556_1557insTATC	ENSP00000395496.2:p.Met520IlefsTer10
ENST00000440875.5:c.1154-168_1154-167insTATC	ENSP00000475553.2:n.1154-168_1154-167insTATC
ENST00000539609.7:c.1397_1398insTATC	ENSP00000443792.2:p.Met467IlefsTer10
ENST00000558170.6:c.1469_1470insTATC	ENSP00000454157.1:p.Met491IlefsTer10
ENST00000627532.2:c.1469_1470insTATC	ENSP00000487174.1:p.Met491IlefsTer10
NM_001171653.1:c.1397_1398insTATC	NP_001165124.1:p.Met467IlefsTer10
NM_014795.3:c.1469_1470insTATC	NP_055610.1:p.Met491IlefsTer10
XM_006712881.2:c.1469_1470insTATC	XP_006712944.1:p.Met491IlefsTer10
XM_006712882.2:c.1469_1470insTATC	XP_006712945.1:p.Met491IlefsTer10
XM_011512231.1:c.1460_1461insTATC	XP_011510533.1:p.Met488IlefsTer10
XM_011512232.1:c.1448_1449insTATC	XP_011510534.1:p.Met484IlefsTer10
NM_014795.4:c.1469_1470insTATC MANE Select	NP_055610.1:p.Met491IlefsTer10
NM_001171653.2:c.1397_1398insTATC	NP_001165124.1:p.Met467IlefsTer10