Canonical Allele Identifier: CA429445886
Gene: ZEB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.145157191G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399624G>C , CM000664.2:g.144399624G>C GRCh38
NC_000002.11:g.145157191G>C , CM000664.1:g.145157191G>C GRCh37
NC_000002.10:g.144873661G>C NCBI36
NG_016431.1:g.125768C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1412C>G ENSP00000508434.1:n.*1412C>G
ENST00000440875.6:c.786C>G ENSP00000475553.3:p.Ala262=
ENST00000627532.3:c.1563C>G MANE Select ENSP00000487174.1:p.Ala521=
ENST00000636026.2:c.1563C>G ENSP00000490776.1:p.Ala521=
ENST00000636179.1:n.1532C>G
ENST00000636413.1:c.1227C>G ENSP00000490508.1:p.Ala409=
ENST00000636471.1:c.1638C>G ENSP00000490317.1:p.Ala546=
ENST00000636732.2:c.*1280C>G ENSP00000490175.1:n.*1280C>G
ENST00000636820.1:n.1663C>G
ENST00000637045.1:c.1227C>G ENSP00000490141.1:p.Ala409=
ENST00000637267.2:c.1563C>G ENSP00000490293.2:p.Ala521=
ENST00000637304.1:c.1227C>G ENSP00000490872.1:p.Ala409=
ENST00000638007.1:c.1227C>G ENSP00000490723.1:p.Ala409=
ENST00000638087.1:c.1227C>G ENSP00000490673.1:p.Ala409=
ENST00000638128.1:c.786C>G ENSP00000490934.1:p.Ala262=
ENST00000675069.1:c.-133-774C>G ENSP00000502467.1:n.-133-774C>G
ENST00000675145.1:n.2111C>G
ENST00000303660.8:c.1560C>G ENSP00000302501.4:p.Ala520=
ENST00000409487.7:c.1563C>G ENSP00000386854.2:p.Ala521=
ENST00000419938.5:c.655+1575C>G ENSP00000394777.2:n.655+1575C>G
ENST00000427902.5:c.1650C>G ENSP00000395496.2:p.Ala550=
ENST00000440875.5:c.1154-74C>G ENSP00000475553.2:n.1154-74C>G
ENST00000539609.7:c.1491C>G ENSP00000443792.2:p.Ala497=
ENST00000558170.6:c.1563C>G ENSP00000454157.1:p.Ala521=
ENST00000627532.2:c.1563C>G ENSP00000487174.1:p.Ala521=
NM_001171653.1:c.1491C>G NP_001165124.1:p.Ala497=
NM_014795.3:c.1563C>G NP_055610.1:p.Ala521=
XM_006712881.2:c.1563C>G XP_006712944.1:p.Ala521=
XM_006712882.2:c.1563C>G XP_006712945.1:p.Ala521=
XM_011512231.1:c.1554C>G XP_011510533.1:p.Ala518=
XM_011512232.1:c.1542C>G XP_011510534.1:p.Ala514=
NM_014795.4:c.1563C>G MANE Select NP_055610.1:p.Ala521=
NM_001171653.2:c.1491C>G NP_001165124.1:p.Ala497=