Canonical Allele Identifier: CA348699516

Gene: ZEB2

Linked Data

• COSMIC: COSM324391
• MyVariant Identifiers: chr2:g.145147308G>A (hg19) ; chr2:g.144389741G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389741G>A , CM000664.2:g.144389741G>A	GRCh38
NC_000002.11:g.145147308G>A , CM000664.1:g.145147308G>A	GRCh37
NC_000002.10:g.144863778G>A	NCBI36
NG_016431.1:g.135651C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3204C>T	ENSP00000508434.1:n.*3204C>T
ENST00000440875.6:c.2578C>T	ENSP00000475553.3:p.Gln860Ter
ENST00000627532.3:c.3355C>T MANE Select	ENSP00000487174.1:p.Gln1119Ter
ENST00000636026.2:c.3243C>T	ENSP00000490776.1:p.Leu1081=
ENST00000636179.1:n.3324C>T
ENST00000636413.1:c.3019C>T	ENSP00000490508.1:p.Gln1007Ter
ENST00000636471.1:c.3430C>T	ENSP00000490317.1:p.Gln1144Ter
ENST00000636732.2:c.*3072C>T	ENSP00000490175.1:n.*3072C>T
ENST00000636820.1:n.3455C>T
ENST00000637045.1:c.3019C>T	ENSP00000490141.1:p.Gln1007Ter
ENST00000637304.1:c.3019C>T	ENSP00000490872.1:p.Gln1007Ter
ENST00000638007.1:c.3019C>T	ENSP00000490723.1:p.Gln1007Ter
ENST00000638087.1:c.3019C>T	ENSP00000490673.1:p.Gln1007Ter
ENST00000638128.1:c.2578C>T	ENSP00000490934.1:p.Gln860Ter
ENST00000639389.1:c.151+6671C>T	ENSP00000492572.1:n.151+6671C>T
ENST00000647488.1:c.575C>T	ENSP00000494820.1:n.575C>T
ENST00000675069.1:c.886C>T	ENSP00000502467.1:p.Gln296Ter
ENST00000303660.8:c.3352C>T	ENSP00000302501.4:p.Gln1118Ter
ENST00000409487.7:c.3355C>T	ENSP00000386854.2:p.Gln1119Ter
ENST00000419938.5:c.656-859C>T	ENSP00000394777.2:n.656-859C>T
ENST00000539609.7:c.3283C>T	ENSP00000443792.2:p.Gln1095Ter
ENST00000558170.6:c.3355C>T	ENSP00000454157.1:p.Gln1119Ter
ENST00000627532.2:c.3355C>T	ENSP00000487174.1:p.Gln1119Ter
NM_001171653.1:c.3283C>T	NP_001165124.1:p.Gln1095Ter
NM_014795.3:c.3355C>T	NP_055610.1:p.Gln1119Ter
XM_006712881.2:c.3355C>T	XP_006712944.1:p.Gln1119Ter
XM_006712882.2:c.3355C>T	XP_006712945.1:p.Gln1119Ter
XM_011512231.1:c.3346C>T	XP_011510533.1:p.Gln1116Ter
XM_011512232.1:c.3334C>T	XP_011510534.1:p.Gln1112Ter
NM_014795.4:c.3355C>T MANE Select	NP_055610.1:p.Gln1119Ter
NM_001171653.2:c.3283C>T	NP_001165124.1:p.Gln1095Ter