Canonical Allele Identifier: CA348704923

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145154147C>G (hg19) ; chr2:g.144396580C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396580C>G , CM000664.2:g.144396580C>G	GRCh38
NC_000002.11:g.145154147C>G , CM000664.1:g.145154147C>G	GRCh37
NC_000002.10:g.144870617C>G	NCBI36
NG_016431.1:g.128812G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2748G>C	ENSP00000508434.1:n.*2748G>C
ENST00000440875.6:c.2122G>C	ENSP00000475553.3:p.Asp708His
ENST00000627532.3:c.2899G>C MANE Select	ENSP00000487174.1:p.Asp967His
ENST00000636026.2:c.2899G>C	ENSP00000490776.1:p.Asp967His
ENST00000636179.1:n.2868G>C
ENST00000636413.1:c.2563G>C	ENSP00000490508.1:p.Asp855His
ENST00000636471.1:c.2974G>C	ENSP00000490317.1:p.Asp992His
ENST00000636732.2:c.*2616G>C	ENSP00000490175.1:n.*2616G>C
ENST00000636820.1:n.2999G>C
ENST00000637045.1:c.2563G>C	ENSP00000490141.1:p.Asp855His
ENST00000637304.1:c.2563G>C	ENSP00000490872.1:p.Asp855His
ENST00000638007.1:c.2563G>C	ENSP00000490723.1:p.Asp855His
ENST00000638087.1:c.2563G>C	ENSP00000490673.1:p.Asp855His
ENST00000638128.1:c.2122G>C	ENSP00000490934.1:p.Asp708His
ENST00000647488.1:c.31G>C	ENSP00000494820.1:p.Asp11His
ENST00000675069.1:c.430G>C	ENSP00000502467.1:p.Asp144His
ENST00000303660.8:c.2896G>C	ENSP00000302501.4:p.Asp966His
ENST00000409487.7:c.2899G>C	ENSP00000386854.2:p.Asp967His
ENST00000419938.5:c.655+4619G>C	ENSP00000394777.2:n.655+4619G>C
ENST00000539609.7:c.2827G>C	ENSP00000443792.2:p.Asp943His
ENST00000558170.6:c.2899G>C	ENSP00000454157.1:p.Asp967His
ENST00000627532.2:c.2899G>C	ENSP00000487174.1:p.Asp967His
NM_001171653.1:c.2827G>C	NP_001165124.1:p.Asp943His
NM_014795.3:c.2899G>C	NP_055610.1:p.Asp967His
XM_006712881.2:c.2899G>C	XP_006712944.1:p.Asp967His
XM_006712882.2:c.2899G>C	XP_006712945.1:p.Asp967His
XM_011512231.1:c.2890G>C	XP_011510533.1:p.Asp964His
XM_011512232.1:c.2878G>C	XP_011510534.1:p.Asp960His
NM_014795.4:c.2899G>C MANE Select	NP_055610.1:p.Asp967His
NM_001171653.2:c.2827G>C	NP_001165124.1:p.Asp943His