Canonical Allele Identifier: CA348704111

Gene: ZEB2

Linked Data

• dbSNP Id: rs1560604995
• MyVariant Identifiers: chr2:g.145154057C>A (hg19) ; chr2:g.144396490C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396490C>A , CM000664.2:g.144396490C>A	GRCh38
NC_000002.11:g.145154057C>A , CM000664.1:g.145154057C>A	GRCh37
NC_000002.10:g.144870527C>A	NCBI36
NG_016431.1:g.128902G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2838G>T	ENSP00000508434.1:n.*2838G>T
ENST00000440875.6:c.2212G>T	ENSP00000475553.3:p.Gly738Cys
ENST00000627532.3:c.2989G>T MANE Select	ENSP00000487174.1:p.Gly997Cys
ENST00000636026.2:c.2989G>T	ENSP00000490776.1:p.Gly997Cys
ENST00000636179.1:n.2958G>T
ENST00000636413.1:c.2653G>T	ENSP00000490508.1:p.Gly885Cys
ENST00000636471.1:c.3064G>T	ENSP00000490317.1:p.Gly1022Cys
ENST00000636732.2:c.*2706G>T	ENSP00000490175.1:n.*2706G>T
ENST00000636820.1:n.3089G>T
ENST00000637045.1:c.2653G>T	ENSP00000490141.1:p.Gly885Cys
ENST00000637304.1:c.2653G>T	ENSP00000490872.1:p.Gly885Cys
ENST00000638007.1:c.2653G>T	ENSP00000490723.1:p.Gly885Cys
ENST00000638087.1:c.2653G>T	ENSP00000490673.1:p.Gly885Cys
ENST00000638128.1:c.2212G>T	ENSP00000490934.1:p.Gly738Cys
ENST00000639389.1:c.73G>T	ENSP00000492572.1:p.Gly25Cys
ENST00000647488.1:c.121G>T	ENSP00000494820.1:p.Gly41Cys
ENST00000675069.1:c.520G>T	ENSP00000502467.1:p.Gly174Cys
ENST00000303660.8:c.2986G>T	ENSP00000302501.4:p.Gly996Cys
ENST00000409487.7:c.2989G>T	ENSP00000386854.2:p.Gly997Cys
ENST00000419938.5:c.655+4709G>T	ENSP00000394777.2:n.655+4709G>T
ENST00000539609.7:c.2917G>T	ENSP00000443792.2:p.Gly973Cys
ENST00000558170.6:c.2989G>T	ENSP00000454157.1:p.Gly997Cys
ENST00000627532.2:c.2989G>T	ENSP00000487174.1:p.Gly997Cys
NM_001171653.1:c.2917G>T	NP_001165124.1:p.Gly973Cys
NM_014795.3:c.2989G>T	NP_055610.1:p.Gly997Cys
XM_006712881.2:c.2989G>T	XP_006712944.1:p.Gly997Cys
XM_006712882.2:c.2989G>T	XP_006712945.1:p.Gly997Cys
XM_011512231.1:c.2980G>T	XP_011510533.1:p.Gly994Cys
XM_011512232.1:c.2968G>T	XP_011510534.1:p.Gly990Cys
NM_014795.4:c.2989G>T MANE Select	NP_055610.1:p.Gly997Cys
NM_001171653.2:c.2917G>T	NP_001165124.1:p.Gly973Cys