Canonical Allele Identifier: CA1294885050

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398849_144398850delinsTC , CM000664.2:g.144398849_144398850delinsTC	GRCh38
NC_000002.11:g.145156416_145156417delinsTC , CM000664.1:g.145156416_145156417delinsTC	GRCh37
NC_000002.10:g.144872886_144872887delinsTC	NCBI36
NG_016431.1:g.126542_126543delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2186_*2187delinsGA	ENSP00000508434.1:n.*2186_*2187delinsGA
ENST00000440875.6:c.1560_1561delinsGA	ENSP00000475553.3:p.Arg520=
ENST00000627532.3:c.2337_2338delinsGA MANE Select	ENSP00000487174.1:p.Arg779=
ENST00000636026.2:c.2337_2338delinsGA	ENSP00000490776.1:p.Arg779=
ENST00000636179.1:n.2306_2307delinsGA
ENST00000636413.1:c.2001_2002delinsGA	ENSP00000490508.1:p.Arg667=
ENST00000636471.1:c.2412_2413delinsGA	ENSP00000490317.1:p.Arg804=
ENST00000636732.2:c.*2054_*2055delinsGA	ENSP00000490175.1:n.*2054_*2055delinsGA
ENST00000636820.1:n.2437_2438delinsGA
ENST00000637045.1:c.2001_2002delinsGA	ENSP00000490141.1:p.Arg667=
ENST00000637304.1:c.2001_2002delinsGA	ENSP00000490872.1:p.Arg667=
ENST00000638007.1:c.2001_2002delinsGA	ENSP00000490723.1:p.Arg667=
ENST00000638087.1:c.2001_2002delinsGA	ENSP00000490673.1:p.Arg667=
ENST00000638128.1:c.1560_1561delinsGA	ENSP00000490934.1:p.Arg520=
ENST00000675069.1:c.-133_-132delinsGA	ENSP00000502467.1:n.-133_-132delinsGA
ENST00000675145.1:n.2885_2886delinsGA
ENST00000303660.8:c.2334_2335delinsGA	ENSP00000302501.4:p.Arg778=
ENST00000409487.7:c.2337_2338delinsGA	ENSP00000386854.2:p.Arg779=
ENST00000419938.5:c.655+2349_655+2350delinsGA	ENSP00000394777.2:n.655+2349_655+2350delinsGA
ENST00000440875.5:c.1167+687_1167+688delinsGA	ENSP00000475553.2:n.1167+687_1167+688delinsGA
ENST00000539609.7:c.2265_2266delinsGA	ENSP00000443792.2:p.Arg755=
ENST00000558170.6:c.2337_2338delinsGA	ENSP00000454157.1:p.Arg779=
ENST00000627532.2:c.2337_2338delinsGA	ENSP00000487174.1:p.Arg779=
NM_001171653.1:c.2265_2266delinsGA	NP_001165124.1:p.Arg755=
NM_014795.3:c.2337_2338delinsGA	NP_055610.1:p.Arg779=
XM_006712881.2:c.2337_2338delinsGA	XP_006712944.1:p.Arg779=
XM_006712882.2:c.2337_2338delinsGA	XP_006712945.1:p.Arg779=
XM_011512231.1:c.2328_2329delinsGA	XP_011510533.1:p.Arg776=
XM_011512232.1:c.2316_2317delinsGA	XP_011510534.1:p.Arg772=
NM_014795.4:c.2337_2338delinsGA MANE Select	NP_055610.1:p.Arg779=
NM_001171653.2:c.2265_2266delinsGA	NP_001165124.1:p.Arg755=