Canonical Allele Identifier: CA429218568

Gene: ZEB2

Linked Data

• gnomAD v4: 2-144404042-C-T
• COSMIC: COSM5672188
• MyVariant Identifiers: chr2:g.145161609C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404042C>T , CM000664.2:g.144404042C>T	GRCh38
NC_000002.11:g.145161609C>T , CM000664.1:g.145161609C>T	GRCh37
NC_000002.10:g.144878079C>T	NCBI36
NG_016431.1:g.121350G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*530G>A	ENSP00000508434.1:n.*530G>A
ENST00000440875.6:c.-97G>A	ENSP00000475553.3:n.-97G>A
ENST00000627532.3:c.681G>A MANE Select	ENSP00000487174.1:p.Lys227=
ENST00000636026.2:c.681G>A	ENSP00000490776.1:p.Lys227=
ENST00000636179.1:n.650G>A
ENST00000636413.1:c.345G>A	ENSP00000490508.1:p.Lys115=
ENST00000636471.1:c.681G>A	ENSP00000490317.1:p.Lys227=
ENST00000636732.2:c.*398G>A	ENSP00000490175.1:n.*398G>A
ENST00000636820.1:n.781G>A
ENST00000637045.1:c.345G>A	ENSP00000490141.1:p.Lys115=
ENST00000637267.2:c.681G>A	ENSP00000490293.2:p.Lys227=
ENST00000637304.1:c.345G>A	ENSP00000490872.1:p.Lys115=
ENST00000638007.1:c.345G>A	ENSP00000490723.1:p.Lys115=
ENST00000638087.1:c.345G>A	ENSP00000490673.1:p.Lys115=
ENST00000638128.1:c.-97G>A	ENSP00000490934.1:n.-97G>A
ENST00000675069.1:c.-133-5192G>A	ENSP00000502467.1:n.-133-5192G>A
ENST00000303660.8:c.678G>A	ENSP00000302501.4:p.Lys226=
ENST00000392861.6:c.765G>A	ENSP00000376601.3:p.Lys255=
ENST00000409487.7:c.681G>A	ENSP00000386854.2:p.Lys227=
ENST00000419938.5:c.420G>A	ENSP00000394777.2:p.Lys140=
ENST00000427902.5:c.768G>A	ENSP00000395496.2:p.Lys256=
ENST00000440875.5:c.666G>A	ENSP00000475553.2:p.Lys222=
ENST00000497268.1:n.627G>A
ENST00000539609.7:c.609G>A	ENSP00000443792.2:p.Lys203=
ENST00000558170.6:c.681G>A	ENSP00000454157.1:p.Lys227=
ENST00000627532.2:c.681G>A	ENSP00000487174.1:p.Lys227=
NM_001171653.1:c.609G>A	NP_001165124.1:p.Lys203=
NM_014795.3:c.681G>A	NP_055610.1:p.Lys227=
XM_006712881.2:c.681G>A	XP_006712944.1:p.Lys227=
XM_006712882.2:c.681G>A	XP_006712945.1:p.Lys227=
XM_011512231.1:c.672G>A	XP_011510533.1:p.Lys224=
XM_011512232.1:c.660G>A	XP_011510534.1:p.Lys220=
NM_014795.4:c.681G>A MANE Select	NP_055610.1:p.Lys227=
NM_001171653.2:c.609G>A	NP_001165124.1:p.Lys203=