Canonical Allele Identifier: CA348714928

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161650G>C (hg19) ; chr2:g.144404083G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404083G>C , CM000664.2:g.144404083G>C	GRCh38
NC_000002.11:g.145161650G>C , CM000664.1:g.145161650G>C	GRCh37
NC_000002.10:g.144878120G>C	NCBI36
NG_016431.1:g.121309C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*489C>G	ENSP00000508434.1:n.*489C>G
ENST00000440875.6:c.-138C>G	ENSP00000475553.3:n.-138C>G
ENST00000627532.3:c.640C>G MANE Select	ENSP00000487174.1:p.Pro214Ala
ENST00000636026.2:c.640C>G	ENSP00000490776.1:p.Pro214Ala
ENST00000636179.1:n.609C>G
ENST00000636413.1:c.304C>G	ENSP00000490508.1:p.Pro102Ala
ENST00000636471.1:c.640C>G	ENSP00000490317.1:p.Pro214Ala
ENST00000636732.2:c.*357C>G	ENSP00000490175.1:n.*357C>G
ENST00000636820.1:n.740C>G
ENST00000637045.1:c.304C>G	ENSP00000490141.1:p.Pro102Ala
ENST00000637267.2:c.640C>G	ENSP00000490293.2:p.Pro214Ala
ENST00000637304.1:c.304C>G	ENSP00000490872.1:p.Pro102Ala
ENST00000638007.1:c.304C>G	ENSP00000490723.1:p.Pro102Ala
ENST00000638087.1:c.304C>G	ENSP00000490673.1:p.Pro102Ala
ENST00000638128.1:c.-138C>G	ENSP00000490934.1:n.-138C>G
ENST00000675069.1:c.-133-5233C>G	ENSP00000502467.1:n.-133-5233C>G
ENST00000303660.8:c.637C>G	ENSP00000302501.4:p.Pro213Ala
ENST00000392861.6:c.724C>G	ENSP00000376601.3:p.Pro242Ala
ENST00000409487.7:c.640C>G	ENSP00000386854.2:p.Pro214Ala
ENST00000419938.5:c.379C>G	ENSP00000394777.2:p.Pro127Ala
ENST00000427902.5:c.727C>G	ENSP00000395496.2:p.Pro243Ala
ENST00000440875.5:c.625C>G	ENSP00000475553.2:p.Pro209Ala
ENST00000497268.1:n.586C>G
ENST00000539609.7:c.568C>G	ENSP00000443792.2:p.Pro190Ala
ENST00000558170.6:c.640C>G	ENSP00000454157.1:p.Pro214Ala
ENST00000627532.2:c.640C>G	ENSP00000487174.1:p.Pro214Ala
NM_001171653.1:c.568C>G	NP_001165124.1:p.Pro190Ala
NM_014795.3:c.640C>G	NP_055610.1:p.Pro214Ala
XM_006712881.2:c.640C>G	XP_006712944.1:p.Pro214Ala
XM_006712882.2:c.640C>G	XP_006712945.1:p.Pro214Ala
XM_011512231.1:c.631C>G	XP_011510533.1:p.Pro211Ala
XM_011512232.1:c.619C>G	XP_011510534.1:p.Pro207Ala
NM_014795.4:c.640C>G MANE Select	NP_055610.1:p.Pro214Ala
NM_001171653.2:c.568C>G	NP_001165124.1:p.Pro190Ala