Canonical Allele Identifier: CA429217653

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145154142T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396575T>C , CM000664.2:g.144396575T>C	GRCh38
NC_000002.11:g.145154142T>C , CM000664.1:g.145154142T>C	GRCh37
NC_000002.10:g.144870612T>C	NCBI36
NG_016431.1:g.128817A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2753A>G	ENSP00000508434.1:n.*2753A>G
ENST00000440875.6:c.2127A>G	ENSP00000475553.3:p.Gly709=
ENST00000627532.3:c.2904A>G MANE Select	ENSP00000487174.1:p.Gly968=
ENST00000636026.2:c.2904A>G	ENSP00000490776.1:p.Gly968=
ENST00000636179.1:n.2873A>G
ENST00000636413.1:c.2568A>G	ENSP00000490508.1:p.Gly856=
ENST00000636471.1:c.2979A>G	ENSP00000490317.1:p.Gly993=
ENST00000636732.2:c.*2621A>G	ENSP00000490175.1:n.*2621A>G
ENST00000636820.1:n.3004A>G
ENST00000637045.1:c.2568A>G	ENSP00000490141.1:p.Gly856=
ENST00000637304.1:c.2568A>G	ENSP00000490872.1:p.Gly856=
ENST00000638007.1:c.2568A>G	ENSP00000490723.1:p.Gly856=
ENST00000638087.1:c.2568A>G	ENSP00000490673.1:p.Gly856=
ENST00000638128.1:c.2127A>G	ENSP00000490934.1:p.Gly709=
ENST00000647488.1:c.36A>G	ENSP00000494820.1:p.Gly12=
ENST00000675069.1:c.435A>G	ENSP00000502467.1:p.Gly145=
ENST00000303660.8:c.2901A>G	ENSP00000302501.4:p.Gly967=
ENST00000409487.7:c.2904A>G	ENSP00000386854.2:p.Gly968=
ENST00000419938.5:c.655+4624A>G	ENSP00000394777.2:n.655+4624A>G
ENST00000539609.7:c.2832A>G	ENSP00000443792.2:p.Gly944=
ENST00000558170.6:c.2904A>G	ENSP00000454157.1:p.Gly968=
ENST00000627532.2:c.2904A>G	ENSP00000487174.1:p.Gly968=
NM_001171653.1:c.2832A>G	NP_001165124.1:p.Gly944=
NM_014795.3:c.2904A>G	NP_055610.1:p.Gly968=
XM_006712881.2:c.2904A>G	XP_006712944.1:p.Gly968=
XM_006712882.2:c.2904A>G	XP_006712945.1:p.Gly968=
XM_011512231.1:c.2895A>G	XP_011510533.1:p.Gly965=
XM_011512232.1:c.2883A>G	XP_011510534.1:p.Gly961=
NM_014795.4:c.2904A>G MANE Select	NP_055610.1:p.Gly968=
NM_001171653.2:c.2832A>G	NP_001165124.1:p.Gly944=