Canonical Allele Identifier: CA1294885368

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399668_144399671delinsTAGG , CM000664.2:g.144399668_144399671delinsTAGG	GRCh38
NC_000002.11:g.145157235_145157238delinsTAGG , CM000664.1:g.145157235_145157238delinsTAGG	GRCh37
NC_000002.10:g.144873705_144873708delinsTAGG	NCBI36
NG_016431.1:g.125721_125724delinsCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1365_*1368delinsCCTA	ENSP00000508434.1:n.*1365_*1368delinsCCTA
ENST00000440875.6:c.739_742delinsCCTA	ENSP00000475553.3:p.Pro247=
ENST00000627532.3:c.1516_1519delinsCCTA MANE Select	ENSP00000487174.1:p.Pro506=
ENST00000636026.2:c.1516_1519delinsCCTA	ENSP00000490776.1:p.Pro506=
ENST00000636179.1:n.1485_1488delinsCCTA
ENST00000636413.1:c.1180_1183delinsCCTA	ENSP00000490508.1:p.Pro394=
ENST00000636471.1:c.1591_1594delinsCCTA	ENSP00000490317.1:p.Pro531=
ENST00000636732.2:c.*1233_*1236delinsCCTA	ENSP00000490175.1:n.*1233_*1236delinsCCTA
ENST00000636820.1:n.1616_1619delinsCCTA
ENST00000637045.1:c.1180_1183delinsCCTA	ENSP00000490141.1:p.Pro394=
ENST00000637267.2:c.1516_1519delinsCCTA	ENSP00000490293.2:p.Pro506=
ENST00000637304.1:c.1180_1183delinsCCTA	ENSP00000490872.1:p.Pro394=
ENST00000638007.1:c.1180_1183delinsCCTA	ENSP00000490723.1:p.Pro394=
ENST00000638087.1:c.1180_1183delinsCCTA	ENSP00000490673.1:p.Pro394=
ENST00000638128.1:c.739_742delinsCCTA	ENSP00000490934.1:p.Pro247=
ENST00000675069.1:c.-133-821_-133-818delinsCCTA	ENSP00000502467.1:n.-133-821_-133-818delinsCCTA
ENST00000675145.1:n.2064_2067delinsCCTA
ENST00000303660.8:c.1513_1516delinsCCTA	ENSP00000302501.4:p.Pro505=
ENST00000409487.7:c.1516_1519delinsCCTA	ENSP00000386854.2:p.Pro506=
ENST00000419938.5:c.655+1528_655+1531delinsCCTA	ENSP00000394777.2:n.655+1528_655+1531delinsCCTA
ENST00000427902.5:c.1603_1606delinsCCTA	ENSP00000395496.2:p.Pro535=
ENST00000440875.5:c.1154-121_1154-118delinsCCTA	ENSP00000475553.2:n.1154-121_1154-118delinsCCTA
ENST00000539609.7:c.1444_1447delinsCCTA	ENSP00000443792.2:p.Pro482=
ENST00000558170.6:c.1516_1519delinsCCTA	ENSP00000454157.1:p.Pro506=
ENST00000627532.2:c.1516_1519delinsCCTA	ENSP00000487174.1:p.Pro506=
NM_001171653.1:c.1444_1447delinsCCTA	NP_001165124.1:p.Pro482=
NM_014795.3:c.1516_1519delinsCCTA	NP_055610.1:p.Pro506=
XM_006712881.2:c.1516_1519delinsCCTA	XP_006712944.1:p.Pro506=
XM_006712882.2:c.1516_1519delinsCCTA	XP_006712945.1:p.Pro506=
XM_011512231.1:c.1507_1510delinsCCTA	XP_011510533.1:p.Pro503=
XM_011512232.1:c.1495_1498delinsCCTA	XP_011510534.1:p.Pro499=
NM_014795.4:c.1516_1519delinsCCTA MANE Select	NP_055610.1:p.Pro506=
NM_001171653.2:c.1444_1447delinsCCTA	NP_001165124.1:p.Pro482=