Canonical Allele Identifier: CA1294885204

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399219_144399221delinsCAT , CM000664.2:g.144399219_144399221delinsCAT	GRCh38
NC_000002.11:g.145156786_145156788delinsCAT , CM000664.1:g.145156786_145156788delinsCAT	GRCh37
NC_000002.10:g.144873256_144873258delinsCAT	NCBI36
NG_016431.1:g.126171_126173delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1815_*1817delinsATG	ENSP00000508434.1:n.*1815_*1817delinsATG
ENST00000440875.6:c.1189_1191delinsATG	ENSP00000475553.3:p.Met397=
ENST00000627532.3:c.1966_1968delinsATG MANE Select	ENSP00000487174.1:p.Met656=
ENST00000636026.2:c.1966_1968delinsATG	ENSP00000490776.1:p.Met656=
ENST00000636179.1:n.1935_1937delinsATG
ENST00000636413.1:c.1630_1632delinsATG	ENSP00000490508.1:p.Met544=
ENST00000636471.1:c.2041_2043delinsATG	ENSP00000490317.1:p.Met681=
ENST00000636732.2:c.*1683_*1685delinsATG	ENSP00000490175.1:n.*1683_*1685delinsATG
ENST00000636820.1:n.2066_2068delinsATG
ENST00000637045.1:c.1630_1632delinsATG	ENSP00000490141.1:p.Met544=
ENST00000637304.1:c.1630_1632delinsATG	ENSP00000490872.1:p.Met544=
ENST00000638007.1:c.1630_1632delinsATG	ENSP00000490723.1:p.Met544=
ENST00000638087.1:c.1630_1632delinsATG	ENSP00000490673.1:p.Met544=
ENST00000638128.1:c.1189_1191delinsATG	ENSP00000490934.1:p.Met397=
ENST00000675069.1:c.-133-371_-133-369delinsATG	ENSP00000502467.1:n.-133-371_-133-369delinsATG
ENST00000675145.1:n.2514_2516delinsATG
ENST00000303660.8:c.1963_1965delinsATG	ENSP00000302501.4:p.Met655=
ENST00000409487.7:c.1966_1968delinsATG	ENSP00000386854.2:p.Met656=
ENST00000419938.5:c.655+1978_655+1980delinsATG	ENSP00000394777.2:n.655+1978_655+1980delinsATG
ENST00000427902.5:c.2053_2055delinsATG	ENSP00000395496.2:p.Met685=
ENST00000440875.5:c.1167+316_1167+318delinsATG	ENSP00000475553.2:n.1167+316_1167+318delinsATG
ENST00000539609.7:c.1894_1896delinsATG	ENSP00000443792.2:p.Met632=
ENST00000558170.6:c.1966_1968delinsATG	ENSP00000454157.1:p.Met656=
ENST00000627532.2:c.1966_1968delinsATG	ENSP00000487174.1:p.Met656=
NM_001171653.1:c.1894_1896delinsATG	NP_001165124.1:p.Met632=
NM_014795.3:c.1966_1968delinsATG	NP_055610.1:p.Met656=
XM_006712881.2:c.1966_1968delinsATG	XP_006712944.1:p.Met656=
XM_006712882.2:c.1966_1968delinsATG	XP_006712945.1:p.Met656=
XM_011512231.1:c.1957_1959delinsATG	XP_011510533.1:p.Met653=
XM_011512232.1:c.1945_1947delinsATG	XP_011510534.1:p.Met649=
NM_014795.4:c.1966_1968delinsATG MANE Select	NP_055610.1:p.Met656=
NM_001171653.2:c.1894_1896delinsATG	NP_001165124.1:p.Met632=