Canonical Allele Identifier: CA1139655625

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 987507
• ClinVar RCV Id: RCV001268920
• dbSNP Id: rs1703258451

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398384dup , CM000664.2:g.144398384dup	GRCh38
NC_000002.11:g.145155951dup , CM000664.1:g.145155951dup	GRCh37
NC_000002.10:g.144872421dup	NCBI36
NG_016431.1:g.127008dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2652dup	ENSP00000508434.1:n.*2652dup
ENST00000440875.6:c.2026dup	ENSP00000475553.3:p.Met676AsnfsTer14
ENST00000627532.3:c.2803dup MANE Select	ENSP00000487174.1:p.Met935AsnfsTer14
ENST00000636026.2:c.2803dup	ENSP00000490776.1:p.Met935AsnfsTer14
ENST00000636179.1:n.2772dup
ENST00000636413.1:c.2467dup	ENSP00000490508.1:p.Met823AsnfsTer14
ENST00000636471.1:c.2878dup	ENSP00000490317.1:p.Met960AsnfsTer14
ENST00000636732.2:c.*2520dup	ENSP00000490175.1:n.*2520dup
ENST00000636820.1:n.2903dup
ENST00000637045.1:c.2467dup	ENSP00000490141.1:p.Met823AsnfsTer14
ENST00000637304.1:c.2467dup	ENSP00000490872.1:p.Met823AsnfsTer14
ENST00000638007.1:c.2467dup	ENSP00000490723.1:p.Met823AsnfsTer14
ENST00000638087.1:c.2467dup	ENSP00000490673.1:p.Met823AsnfsTer14
ENST00000638128.1:c.2026dup	ENSP00000490934.1:p.Met676AsnfsTer14
ENST00000675069.1:c.334dup	ENSP00000502467.1:p.Met112AsnfsTer14
ENST00000303660.8:c.2800dup	ENSP00000302501.4:p.Met934AsnfsTer14
ENST00000409487.7:c.2803dup	ENSP00000386854.2:p.Met935AsnfsTer14
ENST00000419938.5:c.655+2815dup	ENSP00000394777.2:n.655+2815dup
ENST00000440875.5:c.1168-456dup	ENSP00000475553.2:n.1168-456dup
ENST00000539609.7:c.2731dup	ENSP00000443792.2:p.Met911AsnfsTer14
ENST00000558170.6:c.2803dup	ENSP00000454157.1:p.Met935AsnfsTer14
ENST00000627532.2:c.2803dup	ENSP00000487174.1:p.Met935AsnfsTer14
NM_001171653.1:c.2731dup	NP_001165124.1:p.Met911AsnfsTer14
NM_014795.3:c.2803dup	NP_055610.1:p.Met935AsnfsTer14
XM_006712881.2:c.2803dup	XP_006712944.1:p.Met935AsnfsTer14
XM_006712882.2:c.2803dup	XP_006712945.1:p.Met935AsnfsTer14
XM_011512231.1:c.2794dup	XP_011510533.1:p.Met932AsnfsTer14
XM_011512232.1:c.2782dup	XP_011510534.1:p.Met928AsnfsTer14
NM_014795.4:c.2803dup MANE Select	NP_055610.1:p.Met935AsnfsTer14
NM_001171653.2:c.2731dup	NP_001165124.1:p.Met911AsnfsTer14