Canonical Allele Identifier: CA348706756

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145155932G>T (hg19) ; chr2:g.144398365G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398365G>T , CM000664.2:g.144398365G>T	GRCh38
NC_000002.11:g.145155932G>T , CM000664.1:g.145155932G>T	GRCh37
NC_000002.10:g.144872402G>T	NCBI36
NG_016431.1:g.127027C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2671C>A	ENSP00000508434.1:n.*2671C>A
ENST00000440875.6:c.2045C>A	ENSP00000475553.3:p.Thr682Asn
ENST00000627532.3:c.2822C>A MANE Select	ENSP00000487174.1:p.Thr941Asn
ENST00000636026.2:c.2822C>A	ENSP00000490776.1:p.Thr941Asn
ENST00000636179.1:n.2791C>A
ENST00000636413.1:c.2486C>A	ENSP00000490508.1:p.Thr829Asn
ENST00000636471.1:c.2897C>A	ENSP00000490317.1:p.Thr966Asn
ENST00000636732.2:c.*2539C>A	ENSP00000490175.1:n.*2539C>A
ENST00000636820.1:n.2922C>A
ENST00000637045.1:c.2486C>A	ENSP00000490141.1:p.Thr829Asn
ENST00000637304.1:c.2486C>A	ENSP00000490872.1:p.Thr829Asn
ENST00000638007.1:c.2486C>A	ENSP00000490723.1:p.Thr829Asn
ENST00000638087.1:c.2486C>A	ENSP00000490673.1:p.Thr829Asn
ENST00000638128.1:c.2045C>A	ENSP00000490934.1:p.Thr682Asn
ENST00000675069.1:c.353C>A	ENSP00000502467.1:p.Thr118Asn
ENST00000303660.8:c.2819C>A	ENSP00000302501.4:p.Thr940Asn
ENST00000409487.7:c.2822C>A	ENSP00000386854.2:p.Thr941Asn
ENST00000419938.5:c.655+2834C>A	ENSP00000394777.2:n.655+2834C>A
ENST00000440875.5:c.1168-437C>A	ENSP00000475553.2:n.1168-437C>A
ENST00000539609.7:c.2750C>A	ENSP00000443792.2:p.Thr917Asn
ENST00000558170.6:c.2822C>A	ENSP00000454157.1:p.Thr941Asn
ENST00000627532.2:c.2822C>A	ENSP00000487174.1:p.Thr941Asn
NM_001171653.1:c.2750C>A	NP_001165124.1:p.Thr917Asn
NM_014795.3:c.2822C>A	NP_055610.1:p.Thr941Asn
XM_006712881.2:c.2822C>A	XP_006712944.1:p.Thr941Asn
XM_006712882.2:c.2822C>A	XP_006712945.1:p.Thr941Asn
XM_011512231.1:c.2813C>A	XP_011510533.1:p.Thr938Asn
XM_011512232.1:c.2801C>A	XP_011510534.1:p.Thr934Asn
NM_014795.4:c.2822C>A MANE Select	NP_055610.1:p.Thr941Asn
NM_001171653.2:c.2750C>A	NP_001165124.1:p.Thr917Asn