Canonical Allele Identifier: CA429446117

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145157545A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399978A>C , CM000664.2:g.144399978A>C	GRCh38
NC_000002.11:g.145157545A>C , CM000664.1:g.145157545A>C	GRCh37
NC_000002.10:g.144874015A>C	NCBI36
NG_016431.1:g.125414T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1058T>G	ENSP00000508434.1:n.*1058T>G
ENST00000440875.6:c.432T>G	ENSP00000475553.3:p.Leu144=
ENST00000627532.3:c.1209T>G MANE Select	ENSP00000487174.1:p.Leu403=
ENST00000636026.2:c.1209T>G	ENSP00000490776.1:p.Leu403=
ENST00000636179.1:n.1178T>G
ENST00000636413.1:c.873T>G	ENSP00000490508.1:p.Leu291=
ENST00000636471.1:c.1284T>G	ENSP00000490317.1:p.Leu428=
ENST00000636732.2:c.*926T>G	ENSP00000490175.1:n.*926T>G
ENST00000636820.1:n.1309T>G
ENST00000637045.1:c.873T>G	ENSP00000490141.1:p.Leu291=
ENST00000637267.2:c.1209T>G	ENSP00000490293.2:p.Leu403=
ENST00000637304.1:c.873T>G	ENSP00000490872.1:p.Leu291=
ENST00000638007.1:c.873T>G	ENSP00000490723.1:p.Leu291=
ENST00000638087.1:c.873T>G	ENSP00000490673.1:p.Leu291=
ENST00000638128.1:c.432T>G	ENSP00000490934.1:p.Leu144=
ENST00000675069.1:c.-133-1128T>G	ENSP00000502467.1:n.-133-1128T>G
ENST00000675145.1:n.1757T>G
ENST00000303660.8:c.1206T>G	ENSP00000302501.4:p.Leu402=
ENST00000392861.6:c.1293T>G	ENSP00000376601.3:p.Leu431=
ENST00000409487.7:c.1209T>G	ENSP00000386854.2:p.Leu403=
ENST00000419938.5:c.655+1221T>G	ENSP00000394777.2:n.655+1221T>G
ENST00000427902.5:c.1296T>G	ENSP00000395496.2:p.Leu432=
ENST00000440875.5:c.1153+41T>G	ENSP00000475553.2:n.1153+41T>G
ENST00000539609.7:c.1137T>G	ENSP00000443792.2:p.Leu379=
ENST00000558170.6:c.1209T>G	ENSP00000454157.1:p.Leu403=
ENST00000627532.2:c.1209T>G	ENSP00000487174.1:p.Leu403=
NM_001171653.1:c.1137T>G	NP_001165124.1:p.Leu379=
NM_014795.3:c.1209T>G	NP_055610.1:p.Leu403=
XM_006712881.2:c.1209T>G	XP_006712944.1:p.Leu403=
XM_006712882.2:c.1209T>G	XP_006712945.1:p.Leu403=
XM_011512231.1:c.1200T>G	XP_011510533.1:p.Leu400=
XM_011512232.1:c.1188T>G	XP_011510534.1:p.Leu396=
NM_014795.4:c.1209T>G MANE Select	NP_055610.1:p.Leu403=
NM_001171653.2:c.1137T>G	NP_001165124.1:p.Leu379=