Canonical Allele Identifier: CA348706548

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145155886C>A (hg19) ; chr2:g.144398319C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398319C>A , CM000664.2:g.144398319C>A	GRCh38
NC_000002.11:g.145155886C>A , CM000664.1:g.145155886C>A	GRCh37
NC_000002.10:g.144872356C>A	NCBI36
NG_016431.1:g.127073G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2717G>T	ENSP00000508434.1:n.*2717G>T
ENST00000440875.6:c.2091G>T	ENSP00000475553.3:p.Gln697His
ENST00000627532.3:c.2868G>T MANE Select	ENSP00000487174.1:p.Gln956His
ENST00000636026.2:c.2868G>T	ENSP00000490776.1:p.Gln956His
ENST00000636179.1:n.2837G>T
ENST00000636413.1:c.2532G>T	ENSP00000490508.1:p.Gln844His
ENST00000636471.1:c.2943G>T	ENSP00000490317.1:p.Gln981His
ENST00000636732.2:c.*2585G>T	ENSP00000490175.1:n.*2585G>T
ENST00000636820.1:n.2968G>T
ENST00000637045.1:c.2532G>T	ENSP00000490141.1:p.Gln844His
ENST00000637304.1:c.2532G>T	ENSP00000490872.1:p.Gln844His
ENST00000638007.1:c.2532G>T	ENSP00000490723.1:p.Gln844His
ENST00000638087.1:c.2532G>T	ENSP00000490673.1:p.Gln844His
ENST00000638128.1:c.2091G>T	ENSP00000490934.1:p.Gln697His
ENST00000675069.1:c.399G>T	ENSP00000502467.1:p.Gln133His
ENST00000303660.8:c.2865G>T	ENSP00000302501.4:p.Gln955His
ENST00000409487.7:c.2868G>T	ENSP00000386854.2:p.Gln956His
ENST00000419938.5:c.655+2880G>T	ENSP00000394777.2:n.655+2880G>T
ENST00000440875.5:c.1168-391G>T	ENSP00000475553.2:n.1168-391G>T
ENST00000539609.7:c.2796G>T	ENSP00000443792.2:p.Gln932His
ENST00000558170.6:c.2868G>T	ENSP00000454157.1:p.Gln956His
ENST00000627532.2:c.2868G>T	ENSP00000487174.1:p.Gln956His
NM_001171653.1:c.2796G>T	NP_001165124.1:p.Gln932His
NM_014795.3:c.2868G>T	NP_055610.1:p.Gln956His
XM_006712881.2:c.2868G>T	XP_006712944.1:p.Gln956His
XM_006712882.2:c.2868G>T	XP_006712945.1:p.Gln956His
XM_011512231.1:c.2859G>T	XP_011510533.1:p.Gln953His
XM_011512232.1:c.2847G>T	XP_011510534.1:p.Gln949His
NM_014795.4:c.2868G>T MANE Select	NP_055610.1:p.Gln956His
NM_001171653.2:c.2796G>T	NP_001165124.1:p.Gln932His