Canonical Allele Identifier: CA429445582

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156171G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398604G>A , CM000664.2:g.144398604G>A	GRCh38
NC_000002.11:g.145156171G>A , CM000664.1:g.145156171G>A	GRCh37
NC_000002.10:g.144872641G>A	NCBI36
NG_016431.1:g.126788C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2432C>T	ENSP00000508434.1:n.*2432C>T
ENST00000440875.6:c.1806C>T	ENSP00000475553.3:p.Asn602=
ENST00000627532.3:c.2583C>T MANE Select	ENSP00000487174.1:p.Asn861=
ENST00000636026.2:c.2583C>T	ENSP00000490776.1:p.Asn861=
ENST00000636179.1:n.2552C>T
ENST00000636413.1:c.2247C>T	ENSP00000490508.1:p.Asn749=
ENST00000636471.1:c.2658C>T	ENSP00000490317.1:p.Asn886=
ENST00000636732.2:c.*2300C>T	ENSP00000490175.1:n.*2300C>T
ENST00000636820.1:n.2683C>T
ENST00000637045.1:c.2247C>T	ENSP00000490141.1:p.Asn749=
ENST00000637304.1:c.2247C>T	ENSP00000490872.1:p.Asn749=
ENST00000638007.1:c.2247C>T	ENSP00000490723.1:p.Asn749=
ENST00000638087.1:c.2247C>T	ENSP00000490673.1:p.Asn749=
ENST00000638128.1:c.1806C>T	ENSP00000490934.1:p.Asn602=
ENST00000675069.1:c.114C>T	ENSP00000502467.1:p.Asn38=
ENST00000303660.8:c.2580C>T	ENSP00000302501.4:p.Asn860=
ENST00000409487.7:c.2583C>T	ENSP00000386854.2:p.Asn861=
ENST00000419938.5:c.655+2595C>T	ENSP00000394777.2:n.655+2595C>T
ENST00000440875.5:c.1168-676C>T	ENSP00000475553.2:n.1168-676C>T
ENST00000539609.7:c.2511C>T	ENSP00000443792.2:p.Asn837=
ENST00000558170.6:c.2583C>T	ENSP00000454157.1:p.Asn861=
ENST00000627532.2:c.2583C>T	ENSP00000487174.1:p.Asn861=
NM_001171653.1:c.2511C>T	NP_001165124.1:p.Asn837=
NM_014795.3:c.2583C>T	NP_055610.1:p.Asn861=
XM_006712881.2:c.2583C>T	XP_006712944.1:p.Asn861=
XM_006712882.2:c.2583C>T	XP_006712945.1:p.Asn861=
XM_011512231.1:c.2574C>T	XP_011510533.1:p.Asn858=
XM_011512232.1:c.2562C>T	XP_011510534.1:p.Asn854=
NM_014795.4:c.2583C>T MANE Select	NP_055610.1:p.Asn861=
NM_001171653.2:c.2511C>T	NP_001165124.1:p.Asn837=