Canonical Allele Identifier: CA348710188

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156967A>T (hg19) ; chr2:g.144399400A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399400A>T , CM000664.2:g.144399400A>T	GRCh38
NC_000002.11:g.145156967A>T , CM000664.1:g.145156967A>T	GRCh37
NC_000002.10:g.144873437A>T	NCBI36
NG_016431.1:g.125992T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1636T>A	ENSP00000508434.1:n.*1636T>A
ENST00000440875.6:c.1010T>A	ENSP00000475553.3:p.Leu337Ter
ENST00000627532.3:c.1787T>A MANE Select	ENSP00000487174.1:p.Leu596Ter
ENST00000636026.2:c.1787T>A	ENSP00000490776.1:p.Leu596Ter
ENST00000636179.1:n.1756T>A
ENST00000636413.1:c.1451T>A	ENSP00000490508.1:p.Leu484Ter
ENST00000636471.1:c.1862T>A	ENSP00000490317.1:p.Leu621Ter
ENST00000636732.2:c.*1504T>A	ENSP00000490175.1:n.*1504T>A
ENST00000636820.1:n.1887T>A
ENST00000637045.1:c.1451T>A	ENSP00000490141.1:p.Leu484Ter
ENST00000637267.2:c.1787T>A	ENSP00000490293.2:p.Leu596Ter
ENST00000637304.1:c.1451T>A	ENSP00000490872.1:p.Leu484Ter
ENST00000638007.1:c.1451T>A	ENSP00000490723.1:p.Leu484Ter
ENST00000638087.1:c.1451T>A	ENSP00000490673.1:p.Leu484Ter
ENST00000638128.1:c.1010T>A	ENSP00000490934.1:p.Leu337Ter
ENST00000675069.1:c.-133-550T>A	ENSP00000502467.1:n.-133-550T>A
ENST00000675145.1:n.2335T>A
ENST00000303660.8:c.1784T>A	ENSP00000302501.4:p.Leu595Ter
ENST00000409487.7:c.1787T>A	ENSP00000386854.2:p.Leu596Ter
ENST00000419938.5:c.655+1799T>A	ENSP00000394777.2:n.655+1799T>A
ENST00000427902.5:c.1874T>A	ENSP00000395496.2:p.Leu625Ter
ENST00000440875.5:c.1167+137T>A	ENSP00000475553.2:n.1167+137T>A
ENST00000539609.7:c.1715T>A	ENSP00000443792.2:p.Leu572Ter
ENST00000558170.6:c.1787T>A	ENSP00000454157.1:p.Leu596Ter
ENST00000627532.2:c.1787T>A	ENSP00000487174.1:p.Leu596Ter
NM_001171653.1:c.1715T>A	NP_001165124.1:p.Leu572Ter
NM_014795.3:c.1787T>A	NP_055610.1:p.Leu596Ter
XM_006712881.2:c.1787T>A	XP_006712944.1:p.Leu596Ter
XM_006712882.2:c.1787T>A	XP_006712945.1:p.Leu596Ter
XM_011512231.1:c.1778T>A	XP_011510533.1:p.Leu593Ter
XM_011512232.1:c.1766T>A	XP_011510534.1:p.Leu589Ter
NM_014795.4:c.1787T>A MANE Select	NP_055610.1:p.Leu596Ter
NM_001171653.2:c.1715T>A	NP_001165124.1:p.Leu572Ter