Canonical Allele Identifier: CA348704041

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145154047G>A (hg19) ; chr2:g.144396480G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396480G>A , CM000664.2:g.144396480G>A	GRCh38
NC_000002.11:g.145154047G>A , CM000664.1:g.145154047G>A	GRCh37
NC_000002.10:g.144870517G>A	NCBI36
NG_016431.1:g.128912C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2848C>T	ENSP00000508434.1:n.*2848C>T
ENST00000440875.6:c.2222C>T	ENSP00000475553.3:p.Ala741Val
ENST00000627532.3:c.2999C>T MANE Select	ENSP00000487174.1:p.Ala1000Val
ENST00000636026.2:c.2999C>T	ENSP00000490776.1:p.Ala1000Val
ENST00000636179.1:n.2968C>T
ENST00000636413.1:c.2663C>T	ENSP00000490508.1:p.Ala888Val
ENST00000636471.1:c.3074C>T	ENSP00000490317.1:p.Ala1025Val
ENST00000636732.2:c.*2716C>T	ENSP00000490175.1:n.*2716C>T
ENST00000636820.1:n.3099C>T
ENST00000637045.1:c.2663C>T	ENSP00000490141.1:p.Ala888Val
ENST00000637304.1:c.2663C>T	ENSP00000490872.1:p.Ala888Val
ENST00000638007.1:c.2663C>T	ENSP00000490723.1:p.Ala888Val
ENST00000638087.1:c.2663C>T	ENSP00000490673.1:p.Ala888Val
ENST00000638128.1:c.2222C>T	ENSP00000490934.1:p.Ala741Val
ENST00000639389.1:c.83C>T	ENSP00000492572.1:p.Ala28Val
ENST00000647488.1:c.131C>T	ENSP00000494820.1:p.Ala44Val
ENST00000675069.1:c.530C>T	ENSP00000502467.1:p.Ala177Val
ENST00000303660.8:c.2996C>T	ENSP00000302501.4:p.Ala999Val
ENST00000409487.7:c.2999C>T	ENSP00000386854.2:p.Ala1000Val
ENST00000419938.5:c.655+4719C>T	ENSP00000394777.2:n.655+4719C>T
ENST00000539609.7:c.2927C>T	ENSP00000443792.2:p.Ala976Val
ENST00000558170.6:c.2999C>T	ENSP00000454157.1:p.Ala1000Val
ENST00000627532.2:c.2999C>T	ENSP00000487174.1:p.Ala1000Val
NM_001171653.1:c.2927C>T	NP_001165124.1:p.Ala976Val
NM_014795.3:c.2999C>T	NP_055610.1:p.Ala1000Val
XM_006712881.2:c.2999C>T	XP_006712944.1:p.Ala1000Val
XM_006712882.2:c.2999C>T	XP_006712945.1:p.Ala1000Val
XM_011512231.1:c.2990C>T	XP_011510533.1:p.Ala997Val
XM_011512232.1:c.2978C>T	XP_011510534.1:p.Ala993Val
NM_014795.4:c.2999C>T MANE Select	NP_055610.1:p.Ala1000Val
NM_001171653.2:c.2927C>T	NP_001165124.1:p.Ala976Val