Canonical Allele Identifier: CA348706591

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145155901T>A (hg19) ; chr2:g.144398334T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398334T>A , CM000664.2:g.144398334T>A	GRCh38
NC_000002.11:g.145155901T>A , CM000664.1:g.145155901T>A	GRCh37
NC_000002.10:g.144872371T>A	NCBI36
NG_016431.1:g.127058A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2702A>T	ENSP00000508434.1:n.*2702A>T
ENST00000440875.6:c.2076A>T	ENSP00000475553.3:p.Gln692His
ENST00000627532.3:c.2853A>T MANE Select	ENSP00000487174.1:p.Gln951His
ENST00000636026.2:c.2853A>T	ENSP00000490776.1:p.Gln951His
ENST00000636179.1:n.2822A>T
ENST00000636413.1:c.2517A>T	ENSP00000490508.1:p.Gln839His
ENST00000636471.1:c.2928A>T	ENSP00000490317.1:p.Gln976His
ENST00000636732.2:c.*2570A>T	ENSP00000490175.1:n.*2570A>T
ENST00000636820.1:n.2953A>T
ENST00000637045.1:c.2517A>T	ENSP00000490141.1:p.Gln839His
ENST00000637304.1:c.2517A>T	ENSP00000490872.1:p.Gln839His
ENST00000638007.1:c.2517A>T	ENSP00000490723.1:p.Gln839His
ENST00000638087.1:c.2517A>T	ENSP00000490673.1:p.Gln839His
ENST00000638128.1:c.2076A>T	ENSP00000490934.1:p.Gln692His
ENST00000675069.1:c.384A>T	ENSP00000502467.1:p.Gln128His
ENST00000303660.8:c.2850A>T	ENSP00000302501.4:p.Gln950His
ENST00000409487.7:c.2853A>T	ENSP00000386854.2:p.Gln951His
ENST00000419938.5:c.655+2865A>T	ENSP00000394777.2:n.655+2865A>T
ENST00000440875.5:c.1168-406A>T	ENSP00000475553.2:n.1168-406A>T
ENST00000539609.7:c.2781A>T	ENSP00000443792.2:p.Gln927His
ENST00000558170.6:c.2853A>T	ENSP00000454157.1:p.Gln951His
ENST00000627532.2:c.2853A>T	ENSP00000487174.1:p.Gln951His
NM_001171653.1:c.2781A>T	NP_001165124.1:p.Gln927His
NM_014795.3:c.2853A>T	NP_055610.1:p.Gln951His
XM_006712881.2:c.2853A>T	XP_006712944.1:p.Gln951His
XM_006712882.2:c.2853A>T	XP_006712945.1:p.Gln951His
XM_011512231.1:c.2844A>T	XP_011510533.1:p.Gln948His
XM_011512232.1:c.2832A>T	XP_011510534.1:p.Gln944His
NM_014795.4:c.2853A>T MANE Select	NP_055610.1:p.Gln951His
NM_001171653.2:c.2781A>T	NP_001165124.1:p.Gln927His