Canonical Allele Identifier: CA348708449

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156391A>C (hg19) ; chr2:g.144398824A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398824A>C , CM000664.2:g.144398824A>C	GRCh38
NC_000002.11:g.145156391A>C , CM000664.1:g.145156391A>C	GRCh37
NC_000002.10:g.144872861A>C	NCBI36
NG_016431.1:g.126568T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2212T>G	ENSP00000508434.1:n.*2212T>G
ENST00000440875.6:c.1586T>G	ENSP00000475553.3:p.Leu529Arg
ENST00000627532.3:c.2363T>G MANE Select	ENSP00000487174.1:p.Leu788Arg
ENST00000636026.2:c.2363T>G	ENSP00000490776.1:p.Leu788Arg
ENST00000636179.1:n.2332T>G
ENST00000636413.1:c.2027T>G	ENSP00000490508.1:p.Leu676Arg
ENST00000636471.1:c.2438T>G	ENSP00000490317.1:p.Leu813Arg
ENST00000636732.2:c.*2080T>G	ENSP00000490175.1:n.*2080T>G
ENST00000636820.1:n.2463T>G
ENST00000637045.1:c.2027T>G	ENSP00000490141.1:p.Leu676Arg
ENST00000637304.1:c.2027T>G	ENSP00000490872.1:p.Leu676Arg
ENST00000638007.1:c.2027T>G	ENSP00000490723.1:p.Leu676Arg
ENST00000638087.1:c.2027T>G	ENSP00000490673.1:p.Leu676Arg
ENST00000638128.1:c.1586T>G	ENSP00000490934.1:p.Leu529Arg
ENST00000675069.1:c.-107T>G	ENSP00000502467.1:n.-107T>G
ENST00000675145.1:n.2911T>G
ENST00000303660.8:c.2360T>G	ENSP00000302501.4:p.Leu787Arg
ENST00000409487.7:c.2363T>G	ENSP00000386854.2:p.Leu788Arg
ENST00000419938.5:c.655+2375T>G	ENSP00000394777.2:n.655+2375T>G
ENST00000440875.5:c.1167+713T>G	ENSP00000475553.2:n.1167+713T>G
ENST00000539609.7:c.2291T>G	ENSP00000443792.2:p.Leu764Arg
ENST00000558170.6:c.2363T>G	ENSP00000454157.1:p.Leu788Arg
ENST00000627532.2:c.2363T>G	ENSP00000487174.1:p.Leu788Arg
NM_001171653.1:c.2291T>G	NP_001165124.1:p.Leu764Arg
NM_014795.3:c.2363T>G	NP_055610.1:p.Leu788Arg
XM_006712881.2:c.2363T>G	XP_006712944.1:p.Leu788Arg
XM_006712882.2:c.2363T>G	XP_006712945.1:p.Leu788Arg
XM_011512231.1:c.2354T>G	XP_011510533.1:p.Leu785Arg
XM_011512232.1:c.2342T>G	XP_011510534.1:p.Leu781Arg
NM_014795.4:c.2363T>G MANE Select	NP_055610.1:p.Leu788Arg
NM_001171653.2:c.2291T>G	NP_001165124.1:p.Leu764Arg