Canonical Allele Identifier: CA348708486

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156407G>T (hg19) ; chr2:g.144398840G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398840G>T , CM000664.2:g.144398840G>T	GRCh38
NC_000002.11:g.145156407G>T , CM000664.1:g.145156407G>T	GRCh37
NC_000002.10:g.144872877G>T	NCBI36
NG_016431.1:g.126552C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2196C>A	ENSP00000508434.1:n.*2196C>A
ENST00000440875.6:c.1570C>A	ENSP00000475553.3:p.Pro524Thr
ENST00000627532.3:c.2347C>A MANE Select	ENSP00000487174.1:p.Pro783Thr
ENST00000636026.2:c.2347C>A	ENSP00000490776.1:p.Pro783Thr
ENST00000636179.1:n.2316C>A
ENST00000636413.1:c.2011C>A	ENSP00000490508.1:p.Pro671Thr
ENST00000636471.1:c.2422C>A	ENSP00000490317.1:p.Pro808Thr
ENST00000636732.2:c.*2064C>A	ENSP00000490175.1:n.*2064C>A
ENST00000636820.1:n.2447C>A
ENST00000637045.1:c.2011C>A	ENSP00000490141.1:p.Pro671Thr
ENST00000637304.1:c.2011C>A	ENSP00000490872.1:p.Pro671Thr
ENST00000638007.1:c.2011C>A	ENSP00000490723.1:p.Pro671Thr
ENST00000638087.1:c.2011C>A	ENSP00000490673.1:p.Pro671Thr
ENST00000638128.1:c.1570C>A	ENSP00000490934.1:p.Pro524Thr
ENST00000675069.1:c.-123C>A	ENSP00000502467.1:n.-123C>A
ENST00000675145.1:n.2895C>A
ENST00000303660.8:c.2344C>A	ENSP00000302501.4:p.Pro782Thr
ENST00000409487.7:c.2347C>A	ENSP00000386854.2:p.Pro783Thr
ENST00000419938.5:c.655+2359C>A	ENSP00000394777.2:n.655+2359C>A
ENST00000440875.5:c.1167+697C>A	ENSP00000475553.2:n.1167+697C>A
ENST00000539609.7:c.2275C>A	ENSP00000443792.2:p.Pro759Thr
ENST00000558170.6:c.2347C>A	ENSP00000454157.1:p.Pro783Thr
ENST00000627532.2:c.2347C>A	ENSP00000487174.1:p.Pro783Thr
NM_001171653.1:c.2275C>A	NP_001165124.1:p.Pro759Thr
NM_014795.3:c.2347C>A	NP_055610.1:p.Pro783Thr
XM_006712881.2:c.2347C>A	XP_006712944.1:p.Pro783Thr
XM_006712882.2:c.2347C>A	XP_006712945.1:p.Pro783Thr
XM_011512231.1:c.2338C>A	XP_011510533.1:p.Pro780Thr
XM_011512232.1:c.2326C>A	XP_011510534.1:p.Pro776Thr
NM_014795.4:c.2347C>A MANE Select	NP_055610.1:p.Pro783Thr
NM_001171653.2:c.2275C>A	NP_001165124.1:p.Pro759Thr