Canonical Allele Identifier: CA645521253

Gene: ZEB2

Linked Data

• COSMIC: COSM350381

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399850_144399851delinsTT , CM000664.2:g.144399850_144399851delinsTT	GRCh38
NC_000002.11:g.145157417_145157418delinsTT , CM000664.1:g.145157417_145157418delinsTT	GRCh37
NC_000002.10:g.144873887_144873888delinsTT	NCBI36
NG_016431.1:g.125541_125542delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1185_*1186delinsAA	ENSP00000508434.1:n.*1185_*1186delinsAA
ENST00000440875.6:c.559_560delinsAA	ENSP00000475553.3:p.Pro187Asn
ENST00000627532.3:c.1336_1337delinsAA MANE Select	ENSP00000487174.1:p.Pro446Asn
ENST00000636026.2:c.1336_1337delinsAA	ENSP00000490776.1:p.Pro446Asn
ENST00000636179.1:n.1305_1306delinsAA
ENST00000636413.1:c.1000_1001delinsAA	ENSP00000490508.1:p.Pro334Asn
ENST00000636471.1:c.1411_1412delinsAA	ENSP00000490317.1:p.Pro471Asn
ENST00000636732.2:c.*1053_*1054delinsAA	ENSP00000490175.1:n.*1053_*1054delinsAA
ENST00000636820.1:n.1436_1437delinsAA
ENST00000637045.1:c.1000_1001delinsAA	ENSP00000490141.1:p.Pro334Asn
ENST00000637267.2:c.1336_1337delinsAA	ENSP00000490293.2:p.Pro446Asn
ENST00000637304.1:c.1000_1001delinsAA	ENSP00000490872.1:p.Pro334Asn
ENST00000638007.1:c.1000_1001delinsAA	ENSP00000490723.1:p.Pro334Asn
ENST00000638087.1:c.1000_1001delinsAA	ENSP00000490673.1:p.Pro334Asn
ENST00000638128.1:c.559_560delinsAA	ENSP00000490934.1:p.Pro187Asn
ENST00000675069.1:c.-133-1001_-133-1000delinsAA	ENSP00000502467.1:n.-133-1001_-133-1000delinsAA
ENST00000675145.1:n.1884_1885delinsAA
ENST00000303660.8:c.1333_1334delinsAA	ENSP00000302501.4:p.Pro445Asn
ENST00000409487.7:c.1336_1337delinsAA	ENSP00000386854.2:p.Pro446Asn
ENST00000419938.5:c.655+1348_655+1349delinsAA	ENSP00000394777.2:n.655+1348_655+1349delinsAA
ENST00000427902.5:c.1423_1424delinsAA	ENSP00000395496.2:p.Pro475Asn
ENST00000440875.5:c.1153+168_1153+169delinsAA	ENSP00000475553.2:n.1153+168_1153+169delinsAA
ENST00000539609.7:c.1264_1265delinsAA	ENSP00000443792.2:p.Pro422Asn
ENST00000558170.6:c.1336_1337delinsAA	ENSP00000454157.1:p.Pro446Asn
ENST00000627532.2:c.1336_1337delinsAA	ENSP00000487174.1:p.Pro446Asn
NM_001171653.1:c.1264_1265delinsAA	NP_001165124.1:p.Pro422Asn
NM_014795.3:c.1336_1337delinsAA	NP_055610.1:p.Pro446Asn
XM_006712881.2:c.1336_1337delinsAA	XP_006712944.1:p.Pro446Asn
XM_006712882.2:c.1336_1337delinsAA	XP_006712945.1:p.Pro446Asn
XM_011512231.1:c.1327_1328delinsAA	XP_011510533.1:p.Pro443Asn
XM_011512232.1:c.1315_1316delinsAA	XP_011510534.1:p.Pro439Asn
NM_014795.4:c.1336_1337delinsAA MANE Select	NP_055610.1:p.Pro446Asn
NM_001171653.2:c.1264_1265delinsAA	NP_001165124.1:p.Pro422Asn