Canonical Allele Identifier: CA2573051659

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1320108
• ClinVar RCV Id: RCV001775281
• dbSNP Id: rs2149877416

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399979del , CM000664.2:g.144399979del	GRCh38
NC_000002.11:g.145157546del , CM000664.1:g.145157546del	GRCh37
NC_000002.10:g.144874016del	NCBI36
NG_016431.1:g.125414del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1058del	ENSP00000508434.1:n.*1058del
ENST00000440875.6:c.432del	ENSP00000475553.3:p.Met145TrpfsTer13
ENST00000627532.3:c.1209del MANE Select	ENSP00000487174.1:p.Met404TrpfsTer13
ENST00000636026.2:c.1209del	ENSP00000490776.1:p.Met404TrpfsTer13
ENST00000636179.1:n.1178del
ENST00000636413.1:c.873del	ENSP00000490508.1:p.Met292TrpfsTer13
ENST00000636471.1:c.1284del	ENSP00000490317.1:p.Met429TrpfsTer13
ENST00000636732.2:c.*926del	ENSP00000490175.1:n.*926del
ENST00000636820.1:n.1309del
ENST00000637045.1:c.873del	ENSP00000490141.1:p.Met292TrpfsTer13
ENST00000637267.2:c.1209del	ENSP00000490293.2:p.Met404TrpfsTer13
ENST00000637304.1:c.873del	ENSP00000490872.1:p.Met292TrpfsTer13
ENST00000638007.1:c.873del	ENSP00000490723.1:p.Met292TrpfsTer13
ENST00000638087.1:c.873del	ENSP00000490673.1:p.Met292TrpfsTer13
ENST00000638128.1:c.432del	ENSP00000490934.1:p.Met145TrpfsTer13
ENST00000675069.1:c.-133-1128del	ENSP00000502467.1:n.-133-1128del
ENST00000675145.1:n.1757del
ENST00000303660.8:c.1206del	ENSP00000302501.4:p.Met403TrpfsTer13
ENST00000392861.6:c.1293del	ENSP00000376601.3:p.Met432TrpfsTer13
ENST00000409487.7:c.1209del	ENSP00000386854.2:p.Met404TrpfsTer13
ENST00000419938.5:c.655+1221del	ENSP00000394777.2:n.655+1221del
ENST00000427902.5:c.1296del	ENSP00000395496.2:p.Met433TrpfsTer13
ENST00000440875.5:c.1153+41del	ENSP00000475553.2:n.1153+41del
ENST00000539609.7:c.1137del	ENSP00000443792.2:p.Met380TrpfsTer13
ENST00000558170.6:c.1209del	ENSP00000454157.1:p.Met404TrpfsTer13
ENST00000627532.2:c.1209del	ENSP00000487174.1:p.Met404TrpfsTer13
NM_001171653.1:c.1137del	NP_001165124.1:p.Met380TrpfsTer13
NM_014795.3:c.1209del	NP_055610.1:p.Met404TrpfsTer13
XM_006712881.2:c.1209del	XP_006712944.1:p.Met404TrpfsTer13
XM_006712882.2:c.1209del	XP_006712945.1:p.Met404TrpfsTer13
XM_011512231.1:c.1200del	XP_011510533.1:p.Met401TrpfsTer13
XM_011512232.1:c.1188del	XP_011510534.1:p.Met397TrpfsTer13
NM_014795.4:c.1209del MANE Select	NP_055610.1:p.Met404TrpfsTer13
NM_001171653.2:c.1137del	NP_001165124.1:p.Met380TrpfsTer13