Canonical Allele Identifier: CA429445017

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156066T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398499T>G , CM000664.2:g.144398499T>G	GRCh38
NC_000002.11:g.145156066T>G , CM000664.1:g.145156066T>G	GRCh37
NC_000002.10:g.144872536T>G	NCBI36
NG_016431.1:g.126893A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2537A>C	ENSP00000508434.1:n.*2537A>C
ENST00000440875.6:c.1911A>C	ENSP00000475553.3:p.Thr637=
ENST00000627532.3:c.2688A>C MANE Select	ENSP00000487174.1:p.Thr896=
ENST00000636026.2:c.2688A>C	ENSP00000490776.1:p.Thr896=
ENST00000636179.1:n.2657A>C
ENST00000636413.1:c.2352A>C	ENSP00000490508.1:p.Thr784=
ENST00000636471.1:c.2763A>C	ENSP00000490317.1:p.Thr921=
ENST00000636732.2:c.*2405A>C	ENSP00000490175.1:n.*2405A>C
ENST00000636820.1:n.2788A>C
ENST00000637045.1:c.2352A>C	ENSP00000490141.1:p.Thr784=
ENST00000637304.1:c.2352A>C	ENSP00000490872.1:p.Thr784=
ENST00000638007.1:c.2352A>C	ENSP00000490723.1:p.Thr784=
ENST00000638087.1:c.2352A>C	ENSP00000490673.1:p.Thr784=
ENST00000638128.1:c.1911A>C	ENSP00000490934.1:p.Thr637=
ENST00000675069.1:c.219A>C	ENSP00000502467.1:p.Thr73=
ENST00000303660.8:c.2685A>C	ENSP00000302501.4:p.Thr895=
ENST00000409487.7:c.2688A>C	ENSP00000386854.2:p.Thr896=
ENST00000419938.5:c.655+2700A>C	ENSP00000394777.2:n.655+2700A>C
ENST00000440875.5:c.1168-571A>C	ENSP00000475553.2:n.1168-571A>C
ENST00000539609.7:c.2616A>C	ENSP00000443792.2:p.Thr872=
ENST00000558170.6:c.2688A>C	ENSP00000454157.1:p.Thr896=
ENST00000627532.2:c.2688A>C	ENSP00000487174.1:p.Thr896=
NM_001171653.1:c.2616A>C	NP_001165124.1:p.Thr872=
NM_014795.3:c.2688A>C	NP_055610.1:p.Thr896=
XM_006712881.2:c.2688A>C	XP_006712944.1:p.Thr896=
XM_006712882.2:c.2688A>C	XP_006712945.1:p.Thr896=
XM_011512231.1:c.2679A>C	XP_011510533.1:p.Thr893=
XM_011512232.1:c.2667A>C	XP_011510534.1:p.Thr889=
NM_014795.4:c.2688A>C MANE Select	NP_055610.1:p.Thr896=
NM_001171653.2:c.2616A>C	NP_001165124.1:p.Thr872=