Canonical Allele Identifier: CA429441109

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144389634-C-T
• MyVariant Identifiers: chr2:g.145147201C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389634C>T , CM000664.2:g.144389634C>T	GRCh38
NC_000002.11:g.145147201C>T , CM000664.1:g.145147201C>T	GRCh37
NC_000002.10:g.144863671C>T	NCBI36
NG_016431.1:g.135758G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*3311G>A	ENSP00000508434.1:n.*3311G>A
ENST00000440875.6:c.2685G>A	ENSP00000475553.3:p.Gln895=
ENST00000627532.3:c.3462G>A MANE Select	ENSP00000487174.1:p.Gln1154=
ENST00000636026.2:c.3350G>A	ENSP00000490776.1:p.Arg1117Lys
ENST00000636179.1:n.3431G>A
ENST00000636413.1:c.3126G>A	ENSP00000490508.1:p.Gln1042=
ENST00000636471.1:c.3537G>A	ENSP00000490317.1:p.Gln1179=
ENST00000636732.2:c.*3179G>A	ENSP00000490175.1:n.*3179G>A
ENST00000636820.1:n.3562G>A
ENST00000637045.1:c.3126G>A	ENSP00000490141.1:p.Gln1042=
ENST00000637304.1:c.3126G>A	ENSP00000490872.1:p.Gln1042=
ENST00000638007.1:c.3126G>A	ENSP00000490723.1:p.Gln1042=
ENST00000638087.1:c.3126G>A	ENSP00000490673.1:p.Gln1042=
ENST00000638128.1:c.2685G>A	ENSP00000490934.1:p.Gln895=
ENST00000639389.1:c.151+6778G>A	ENSP00000492572.1:n.151+6778G>A
ENST00000647488.1:c.682G>A	ENSP00000494820.1:n.682G>A
ENST00000675069.1:c.993G>A	ENSP00000502467.1:p.Gln331=
ENST00000303660.8:c.3459G>A	ENSP00000302501.4:p.Gln1153=
ENST00000409487.7:c.3462G>A	ENSP00000386854.2:p.Gln1154=
ENST00000419938.5:c.656-752G>A	ENSP00000394777.2:n.656-752G>A
ENST00000539609.7:c.3390G>A	ENSP00000443792.2:p.Gln1130=
ENST00000558170.6:c.3462G>A	ENSP00000454157.1:p.Gln1154=
ENST00000627532.2:c.3462G>A	ENSP00000487174.1:p.Gln1154=
NM_001171653.1:c.3390G>A	NP_001165124.1:p.Gln1130=
NM_014795.3:c.3462G>A	NP_055610.1:p.Gln1154=
XM_006712881.2:c.3462G>A	XP_006712944.1:p.Gln1154=
XM_006712882.2:c.3462G>A	XP_006712945.1:p.Gln1154=
XM_011512231.1:c.3453G>A	XP_011510533.1:p.Gln1151=
XM_011512232.1:c.3441G>A	XP_011510534.1:p.Gln1147=
NM_014795.4:c.3462G>A MANE Select	NP_055610.1:p.Gln1154=
NM_001171653.2:c.3390G>A	NP_001165124.1:p.Gln1130=