Canonical Allele Identifier: CA348714666

Gene: ZEB2

Linked Data

• COSMIC: COSM5058118
• MyVariant Identifiers: chr2:g.145161536A>G (hg19) ; chr2:g.144403969A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403969A>G , CM000664.2:g.144403969A>G	GRCh38
NC_000002.11:g.145161536A>G , CM000664.1:g.145161536A>G	GRCh37
NC_000002.10:g.144878006A>G	NCBI36
NG_016431.1:g.121423T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*603T>C	ENSP00000508434.1:n.*603T>C
ENST00000440875.6:c.-24T>C	ENSP00000475553.3:n.-24T>C
ENST00000627532.3:c.754T>C MANE Select	ENSP00000487174.1:p.Tyr252His
ENST00000636026.2:c.754T>C	ENSP00000490776.1:p.Tyr252His
ENST00000636179.1:n.723T>C
ENST00000636413.1:c.418T>C	ENSP00000490508.1:p.Tyr140His
ENST00000636471.1:c.754T>C	ENSP00000490317.1:p.Tyr252His
ENST00000636732.2:c.*471T>C	ENSP00000490175.1:n.*471T>C
ENST00000636820.1:n.854T>C
ENST00000637045.1:c.418T>C	ENSP00000490141.1:p.Tyr140His
ENST00000637267.2:c.754T>C	ENSP00000490293.2:p.Tyr252His
ENST00000637304.1:c.418T>C	ENSP00000490872.1:p.Tyr140His
ENST00000638007.1:c.418T>C	ENSP00000490723.1:p.Tyr140His
ENST00000638087.1:c.418T>C	ENSP00000490673.1:p.Tyr140His
ENST00000638128.1:c.-24T>C	ENSP00000490934.1:n.-24T>C
ENST00000675069.1:c.-133-5119T>C	ENSP00000502467.1:n.-133-5119T>C
ENST00000303660.8:c.751T>C	ENSP00000302501.4:p.Tyr251His
ENST00000392861.6:c.838T>C	ENSP00000376601.3:p.Tyr280His
ENST00000409487.7:c.754T>C	ENSP00000386854.2:p.Tyr252His
ENST00000419938.5:c.493T>C	ENSP00000394777.2:p.Tyr165His
ENST00000427902.5:c.841T>C	ENSP00000395496.2:p.Tyr281His
ENST00000440875.5:c.739T>C	ENSP00000475553.2:p.Tyr247His
ENST00000539609.7:c.682T>C	ENSP00000443792.2:p.Tyr228His
ENST00000558170.6:c.754T>C	ENSP00000454157.1:p.Tyr252His
ENST00000627532.2:c.754T>C	ENSP00000487174.1:p.Tyr252His
NM_001171653.1:c.682T>C	NP_001165124.1:p.Tyr228His
NM_014795.3:c.754T>C	NP_055610.1:p.Tyr252His
XM_006712881.2:c.754T>C	XP_006712944.1:p.Tyr252His
XM_006712882.2:c.754T>C	XP_006712945.1:p.Tyr252His
XM_011512231.1:c.745T>C	XP_011510533.1:p.Tyr249His
XM_011512232.1:c.733T>C	XP_011510534.1:p.Tyr245His
NM_014795.4:c.754T>C MANE Select	NP_055610.1:p.Tyr252His
NM_001171653.2:c.682T>C	NP_001165124.1:p.Tyr228His