Canonical Allele Identifier: CA348711147

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145157222A>C (hg19) ; chr2:g.144399655A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399655A>C , CM000664.2:g.144399655A>C	GRCh38
NC_000002.11:g.145157222A>C , CM000664.1:g.145157222A>C	GRCh37
NC_000002.10:g.144873692A>C	NCBI36
NG_016431.1:g.125737T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1381T>G	ENSP00000508434.1:n.*1381T>G
ENST00000440875.6:c.755T>G	ENSP00000475553.3:p.Val252Gly
ENST00000627532.3:c.1532T>G MANE Select	ENSP00000487174.1:p.Val511Gly
ENST00000636026.2:c.1532T>G	ENSP00000490776.1:p.Val511Gly
ENST00000636179.1:n.1501T>G
ENST00000636413.1:c.1196T>G	ENSP00000490508.1:p.Val399Gly
ENST00000636471.1:c.1607T>G	ENSP00000490317.1:p.Val536Gly
ENST00000636732.2:c.*1249T>G	ENSP00000490175.1:n.*1249T>G
ENST00000636820.1:n.1632T>G
ENST00000637045.1:c.1196T>G	ENSP00000490141.1:p.Val399Gly
ENST00000637267.2:c.1532T>G	ENSP00000490293.2:p.Val511Gly
ENST00000637304.1:c.1196T>G	ENSP00000490872.1:p.Val399Gly
ENST00000638007.1:c.1196T>G	ENSP00000490723.1:p.Val399Gly
ENST00000638087.1:c.1196T>G	ENSP00000490673.1:p.Val399Gly
ENST00000638128.1:c.755T>G	ENSP00000490934.1:p.Val252Gly
ENST00000675069.1:c.-133-805T>G	ENSP00000502467.1:n.-133-805T>G
ENST00000675145.1:n.2080T>G
ENST00000303660.8:c.1529T>G	ENSP00000302501.4:p.Val510Gly
ENST00000409487.7:c.1532T>G	ENSP00000386854.2:p.Val511Gly
ENST00000419938.5:c.655+1544T>G	ENSP00000394777.2:n.655+1544T>G
ENST00000427902.5:c.1619T>G	ENSP00000395496.2:p.Val540Gly
ENST00000440875.5:c.1154-105T>G	ENSP00000475553.2:n.1154-105T>G
ENST00000539609.7:c.1460T>G	ENSP00000443792.2:p.Val487Gly
ENST00000558170.6:c.1532T>G	ENSP00000454157.1:p.Val511Gly
ENST00000627532.2:c.1532T>G	ENSP00000487174.1:p.Val511Gly
NM_001171653.1:c.1460T>G	NP_001165124.1:p.Val487Gly
NM_014795.3:c.1532T>G	NP_055610.1:p.Val511Gly
XM_006712881.2:c.1532T>G	XP_006712944.1:p.Val511Gly
XM_006712882.2:c.1532T>G	XP_006712945.1:p.Val511Gly
XM_011512231.1:c.1523T>G	XP_011510533.1:p.Val508Gly
XM_011512232.1:c.1511T>G	XP_011510534.1:p.Val504Gly
NM_014795.4:c.1532T>G MANE Select	NP_055610.1:p.Val511Gly
NM_001171653.2:c.1460T>G	NP_001165124.1:p.Val487Gly