Canonical Allele Identifier: CA429218512

Gene: ZEB2

Linked Data

• dbSNP Id: rs1431555828
• gnomAD v2: 2-145161555-G-C
• COSMIC: COSM6087838
• MyVariant Identifiers: chr2:g.145161555G>C (hg19) ; chr2:g.144403988G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403988G>C , CM000664.2:g.144403988G>C	GRCh38
NC_000002.11:g.145161555G>C , CM000664.1:g.145161555G>C	GRCh37
NC_000002.10:g.144878025G>C	NCBI36
NG_016431.1:g.121404C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*584C>G	ENSP00000508434.1:n.*584C>G
ENST00000440875.6:c.-43C>G	ENSP00000475553.3:n.-43C>G
ENST00000627532.3:c.735C>G MANE Select	ENSP00000487174.1:p.Leu245=
ENST00000636026.2:c.735C>G	ENSP00000490776.1:p.Leu245=
ENST00000636179.1:n.704C>G
ENST00000636413.1:c.399C>G	ENSP00000490508.1:p.Leu133=
ENST00000636471.1:c.735C>G	ENSP00000490317.1:p.Leu245=
ENST00000636732.2:c.*452C>G	ENSP00000490175.1:n.*452C>G
ENST00000636820.1:n.835C>G
ENST00000637045.1:c.399C>G	ENSP00000490141.1:p.Leu133=
ENST00000637267.2:c.735C>G	ENSP00000490293.2:p.Leu245=
ENST00000637304.1:c.399C>G	ENSP00000490872.1:p.Leu133=
ENST00000638007.1:c.399C>G	ENSP00000490723.1:p.Leu133=
ENST00000638087.1:c.399C>G	ENSP00000490673.1:p.Leu133=
ENST00000638128.1:c.-43C>G	ENSP00000490934.1:n.-43C>G
ENST00000675069.1:c.-133-5138C>G	ENSP00000502467.1:n.-133-5138C>G
ENST00000303660.8:c.732C>G	ENSP00000302501.4:p.Leu244=
ENST00000392861.6:c.819C>G	ENSP00000376601.3:p.Leu273=
ENST00000409487.7:c.735C>G	ENSP00000386854.2:p.Leu245=
ENST00000419938.5:c.474C>G	ENSP00000394777.2:p.Leu158=
ENST00000427902.5:c.822C>G	ENSP00000395496.2:p.Leu274=
ENST00000440875.5:c.720C>G	ENSP00000475553.2:p.Leu240=
ENST00000539609.7:c.663C>G	ENSP00000443792.2:p.Leu221=
ENST00000558170.6:c.735C>G	ENSP00000454157.1:p.Leu245=
ENST00000627532.2:c.735C>G	ENSP00000487174.1:p.Leu245=
NM_001171653.1:c.663C>G	NP_001165124.1:p.Leu221=
NM_014795.3:c.735C>G	NP_055610.1:p.Leu245=
XM_006712881.2:c.735C>G	XP_006712944.1:p.Leu245=
XM_006712882.2:c.735C>G	XP_006712945.1:p.Leu245=
XM_011512231.1:c.726C>G	XP_011510533.1:p.Leu242=
XM_011512232.1:c.714C>G	XP_011510534.1:p.Leu238=
NM_014795.4:c.735C>G MANE Select	NP_055610.1:p.Leu245=
NM_001171653.2:c.663C>G	NP_001165124.1:p.Leu221=