Canonical Allele Identifier: CA348712045

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145157402G>T (hg19) ; chr2:g.144399835G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399835G>T , CM000664.2:g.144399835G>T	GRCh38
NC_000002.11:g.145157402G>T , CM000664.1:g.145157402G>T	GRCh37
NC_000002.10:g.144873872G>T	NCBI36
NG_016431.1:g.125557C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1201C>A	ENSP00000508434.1:n.*1201C>A
ENST00000440875.6:c.575C>A	ENSP00000475553.3:p.Pro192His
ENST00000627532.3:c.1352C>A MANE Select	ENSP00000487174.1:p.Pro451His
ENST00000636026.2:c.1352C>A	ENSP00000490776.1:p.Pro451His
ENST00000636179.1:n.1321C>A
ENST00000636413.1:c.1016C>A	ENSP00000490508.1:p.Pro339His
ENST00000636471.1:c.1427C>A	ENSP00000490317.1:p.Pro476His
ENST00000636732.2:c.*1069C>A	ENSP00000490175.1:n.*1069C>A
ENST00000636820.1:n.1452C>A
ENST00000637045.1:c.1016C>A	ENSP00000490141.1:p.Pro339His
ENST00000637267.2:c.1352C>A	ENSP00000490293.2:p.Pro451His
ENST00000637304.1:c.1016C>A	ENSP00000490872.1:p.Pro339His
ENST00000638007.1:c.1016C>A	ENSP00000490723.1:p.Pro339His
ENST00000638087.1:c.1016C>A	ENSP00000490673.1:p.Pro339His
ENST00000638128.1:c.575C>A	ENSP00000490934.1:p.Pro192His
ENST00000675069.1:c.-133-985C>A	ENSP00000502467.1:n.-133-985C>A
ENST00000675145.1:n.1900C>A
ENST00000303660.8:c.1349C>A	ENSP00000302501.4:p.Pro450His
ENST00000409487.7:c.1352C>A	ENSP00000386854.2:p.Pro451His
ENST00000419938.5:c.655+1364C>A	ENSP00000394777.2:n.655+1364C>A
ENST00000427902.5:c.1439C>A	ENSP00000395496.2:p.Pro480His
ENST00000440875.5:c.1153+184C>A	ENSP00000475553.2:n.1153+184C>A
ENST00000539609.7:c.1280C>A	ENSP00000443792.2:p.Pro427His
ENST00000558170.6:c.1352C>A	ENSP00000454157.1:p.Pro451His
ENST00000627532.2:c.1352C>A	ENSP00000487174.1:p.Pro451His
NM_001171653.1:c.1280C>A	NP_001165124.1:p.Pro427His
NM_014795.3:c.1352C>A	NP_055610.1:p.Pro451His
XM_006712881.2:c.1352C>A	XP_006712944.1:p.Pro451His
XM_006712882.2:c.1352C>A	XP_006712945.1:p.Pro451His
XM_011512231.1:c.1343C>A	XP_011510533.1:p.Pro448His
XM_011512232.1:c.1331C>A	XP_011510534.1:p.Pro444His
NM_014795.4:c.1352C>A MANE Select	NP_055610.1:p.Pro451His
NM_001171653.2:c.1280C>A	NP_001165124.1:p.Pro427His