Canonical Allele Identifier: CA348711322

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145157286G>A (hg19) ; chr2:g.144399719G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399719G>A , CM000664.2:g.144399719G>A	GRCh38
NC_000002.11:g.145157286G>A , CM000664.1:g.145157286G>A	GRCh37
NC_000002.10:g.144873756G>A	NCBI36
NG_016431.1:g.125673C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1317C>T	ENSP00000508434.1:n.*1317C>T
ENST00000440875.6:c.691C>T	ENSP00000475553.3:p.His231Tyr
ENST00000627532.3:c.1468C>T MANE Select	ENSP00000487174.1:p.His490Tyr
ENST00000636026.2:c.1468C>T	ENSP00000490776.1:p.His490Tyr
ENST00000636179.1:n.1437C>T
ENST00000636413.1:c.1132C>T	ENSP00000490508.1:p.His378Tyr
ENST00000636471.1:c.1543C>T	ENSP00000490317.1:p.His515Tyr
ENST00000636732.2:c.*1185C>T	ENSP00000490175.1:n.*1185C>T
ENST00000636820.1:n.1568C>T
ENST00000637045.1:c.1132C>T	ENSP00000490141.1:p.His378Tyr
ENST00000637267.2:c.1468C>T	ENSP00000490293.2:p.His490Tyr
ENST00000637304.1:c.1132C>T	ENSP00000490872.1:p.His378Tyr
ENST00000638007.1:c.1132C>T	ENSP00000490723.1:p.His378Tyr
ENST00000638087.1:c.1132C>T	ENSP00000490673.1:p.His378Tyr
ENST00000638128.1:c.691C>T	ENSP00000490934.1:p.His231Tyr
ENST00000675069.1:c.-133-869C>T	ENSP00000502467.1:n.-133-869C>T
ENST00000675145.1:n.2016C>T
ENST00000303660.8:c.1465C>T	ENSP00000302501.4:p.His489Tyr
ENST00000409487.7:c.1468C>T	ENSP00000386854.2:p.His490Tyr
ENST00000419938.5:c.655+1480C>T	ENSP00000394777.2:n.655+1480C>T
ENST00000427902.5:c.1555C>T	ENSP00000395496.2:p.His519Tyr
ENST00000440875.5:c.1154-169C>T	ENSP00000475553.2:n.1154-169C>T
ENST00000539609.7:c.1396C>T	ENSP00000443792.2:p.His466Tyr
ENST00000558170.6:c.1468C>T	ENSP00000454157.1:p.His490Tyr
ENST00000627532.2:c.1468C>T	ENSP00000487174.1:p.His490Tyr
NM_001171653.1:c.1396C>T	NP_001165124.1:p.His466Tyr
NM_014795.3:c.1468C>T	NP_055610.1:p.His490Tyr
XM_006712881.2:c.1468C>T	XP_006712944.1:p.His490Tyr
XM_006712882.2:c.1468C>T	XP_006712945.1:p.His490Tyr
XM_011512231.1:c.1459C>T	XP_011510533.1:p.His487Tyr
XM_011512232.1:c.1447C>T	XP_011510534.1:p.His483Tyr
NM_014795.4:c.1468C>T MANE Select	NP_055610.1:p.His490Tyr
NM_001171653.2:c.1396C>T	NP_001165124.1:p.His466Tyr