Canonical Allele Identifier: CA348708300

Gene: ZEB2

Linked Data

• dbSNP Id: rs1573715706
• MyVariant Identifiers: chr2:g.145156323G>C (hg19) ; chr2:g.144398756G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398756G>C , CM000664.2:g.144398756G>C	GRCh38
NC_000002.11:g.145156323G>C , CM000664.1:g.145156323G>C	GRCh37
NC_000002.10:g.144872793G>C	NCBI36
NG_016431.1:g.126636C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2280C>G	ENSP00000508434.1:n.*2280C>G
ENST00000440875.6:c.1654C>G	ENSP00000475553.3:p.Leu552Val
ENST00000627532.3:c.2431C>G MANE Select	ENSP00000487174.1:p.Leu811Val
ENST00000636026.2:c.2431C>G	ENSP00000490776.1:p.Leu811Val
ENST00000636179.1:n.2400C>G
ENST00000636413.1:c.2095C>G	ENSP00000490508.1:p.Leu699Val
ENST00000636471.1:c.2506C>G	ENSP00000490317.1:p.Leu836Val
ENST00000636732.2:c.*2148C>G	ENSP00000490175.1:n.*2148C>G
ENST00000636820.1:n.2531C>G
ENST00000637045.1:c.2095C>G	ENSP00000490141.1:p.Leu699Val
ENST00000637304.1:c.2095C>G	ENSP00000490872.1:p.Leu699Val
ENST00000638007.1:c.2095C>G	ENSP00000490723.1:p.Leu699Val
ENST00000638087.1:c.2095C>G	ENSP00000490673.1:p.Leu699Val
ENST00000638128.1:c.1654C>G	ENSP00000490934.1:p.Leu552Val
ENST00000675069.1:c.-39C>G	ENSP00000502467.1:n.-39C>G
ENST00000675145.1:n.2979C>G
ENST00000303660.8:c.2428C>G	ENSP00000302501.4:p.Leu810Val
ENST00000409487.7:c.2431C>G	ENSP00000386854.2:p.Leu811Val
ENST00000419938.5:c.655+2443C>G	ENSP00000394777.2:n.655+2443C>G
ENST00000440875.5:c.1167+781C>G	ENSP00000475553.2:n.1167+781C>G
ENST00000539609.7:c.2359C>G	ENSP00000443792.2:p.Leu787Val
ENST00000558170.6:c.2431C>G	ENSP00000454157.1:p.Leu811Val
ENST00000627532.2:c.2431C>G	ENSP00000487174.1:p.Leu811Val
NM_001171653.1:c.2359C>G	NP_001165124.1:p.Leu787Val
NM_014795.3:c.2431C>G	NP_055610.1:p.Leu811Val
XM_006712881.2:c.2431C>G	XP_006712944.1:p.Leu811Val
XM_006712882.2:c.2431C>G	XP_006712945.1:p.Leu811Val
XM_011512231.1:c.2422C>G	XP_011510533.1:p.Leu808Val
XM_011512232.1:c.2410C>G	XP_011510534.1:p.Leu804Val
NM_014795.4:c.2431C>G MANE Select	NP_055610.1:p.Leu811Val
NM_001171653.2:c.2359C>G	NP_001165124.1:p.Leu787Val