Canonical Allele Identifier: CA348714992

Gene: ZEB2

Linked Data

• COSMIC: COSM5860195
• MyVariant Identifiers: chr2:g.145161680G>A (hg19) ; chr2:g.144404113G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404113G>A , CM000664.2:g.144404113G>A	GRCh38
NC_000002.11:g.145161680G>A , CM000664.1:g.145161680G>A	GRCh37
NC_000002.10:g.144878150G>A	NCBI36
NG_016431.1:g.121279C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*459C>T	ENSP00000508434.1:n.*459C>T
ENST00000440875.6:c.-168C>T	ENSP00000475553.3:n.-168C>T
ENST00000627532.3:c.610C>T MANE Select	ENSP00000487174.1:p.Pro204Ser
ENST00000636026.2:c.610C>T	ENSP00000490776.1:p.Pro204Ser
ENST00000636179.1:n.579C>T
ENST00000636413.1:c.274C>T	ENSP00000490508.1:p.Pro92Ser
ENST00000636471.1:c.610C>T	ENSP00000490317.1:p.Pro204Ser
ENST00000636732.2:c.*327C>T	ENSP00000490175.1:n.*327C>T
ENST00000636820.1:n.710C>T
ENST00000637045.1:c.274C>T	ENSP00000490141.1:p.Pro92Ser
ENST00000637267.2:c.610C>T	ENSP00000490293.2:p.Pro204Ser
ENST00000637304.1:c.274C>T	ENSP00000490872.1:p.Pro92Ser
ENST00000638007.1:c.274C>T	ENSP00000490723.1:p.Pro92Ser
ENST00000638087.1:c.274C>T	ENSP00000490673.1:p.Pro92Ser
ENST00000638128.1:c.-168C>T	ENSP00000490934.1:n.-168C>T
ENST00000675069.1:c.-133-5263C>T	ENSP00000502467.1:n.-133-5263C>T
ENST00000303660.8:c.607C>T	ENSP00000302501.4:p.Pro203Ser
ENST00000392861.6:c.694C>T	ENSP00000376601.3:p.Pro232Ser
ENST00000409487.7:c.610C>T	ENSP00000386854.2:p.Pro204Ser
ENST00000419938.5:c.349C>T	ENSP00000394777.2:p.Pro117Ser
ENST00000427902.5:c.697C>T	ENSP00000395496.2:p.Pro233Ser
ENST00000431672.4:c.538C>T	ENSP00000475267.2:p.Pro180Ser
ENST00000440875.5:c.595C>T	ENSP00000475553.2:p.Pro199Ser
ENST00000497268.1:n.556C>T
ENST00000539609.7:c.538C>T	ENSP00000443792.2:p.Pro180Ser
ENST00000558170.6:c.610C>T	ENSP00000454157.1:p.Pro204Ser
ENST00000627532.2:c.610C>T	ENSP00000487174.1:p.Pro204Ser
ENST00000627856.2:n.570C>T
NM_001171653.1:c.538C>T	NP_001165124.1:p.Pro180Ser
NM_014795.3:c.610C>T	NP_055610.1:p.Pro204Ser
XM_006712881.2:c.610C>T	XP_006712944.1:p.Pro204Ser
XM_006712882.2:c.610C>T	XP_006712945.1:p.Pro204Ser
XM_011512231.1:c.601C>T	XP_011510533.1:p.Pro201Ser
XM_011512232.1:c.589C>T	XP_011510534.1:p.Pro197Ser
NM_014795.4:c.610C>T MANE Select	NP_055610.1:p.Pro204Ser
NM_001171653.2:c.538C>T	NP_001165124.1:p.Pro180Ser