Canonical Allele Identifier: CA758235373

Gene: ZEB2

Linked Data

• dbSNP Id: rs1247290739
• MyVariant Identifiers: chr2:g.145146372C>T (hg19) ; chr2:g.144388805C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144388805C>T , CM000664.2:g.144388805C>T	GRCh38
NC_000002.11:g.145146372C>T , CM000664.1:g.145146372C>T	GRCh37
NC_000002.10:g.144862842C>T	NCBI36
NG_016431.1:g.136587G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440875.6:c.*646G>A	ENSP00000475553.3:n.*646G>A
ENST00000627532.3:c.*646G>A MANE Select	ENSP00000487174.1:n.*646G>A
ENST00000636026.2:c.*570G>A	ENSP00000490776.1:n.*570G>A
ENST00000636179.1:n.4260G>A
ENST00000636413.1:c.*646G>A	ENSP00000490508.1:n.*646G>A
ENST00000636471.1:c.*646G>A	ENSP00000490317.1:n.*646G>A
ENST00000636732.2:c.*4008G>A	ENSP00000490175.1:n.*4008G>A
ENST00000636820.1:n.4391G>A
ENST00000637045.1:c.*646G>A	ENSP00000490141.1:n.*646G>A
ENST00000637304.1:c.*646G>A	ENSP00000490872.1:n.*646G>A
ENST00000638007.1:c.*646G>A	ENSP00000490723.1:n.*646G>A
ENST00000638087.1:c.*646G>A	ENSP00000490673.1:n.*646G>A
ENST00000638128.1:c.*646G>A	ENSP00000490934.1:n.*646G>A
ENST00000639389.1:c.151+7607G>A	ENSP00000492572.1:n.151+7607G>A
ENST00000647488.1:c.1511G>A	ENSP00000494820.1:n.1511G>A
ENST00000675069.1:c.*646G>A	ENSP00000502467.1:n.*646G>A
ENST00000409487.7:c.*646G>A	ENSP00000386854.2:n.*646G>A
ENST00000419938.5:c.*70G>A	ENSP00000394777.2:n.*70G>A
ENST00000627532.2:c.*646G>A	ENSP00000487174.1:n.*646G>A
NM_001171653.1:c.*646G>A	NP_001165124.1:n.*646G>A
NM_014795.3:c.*646G>A	NP_055610.1:n.*646G>A
XM_006712881.2:c.*646G>A	XP_006712944.1:n.*646G>A
XM_006712882.2:c.*646G>A	XP_006712945.1:n.*646G>A
XM_011512231.1:c.*646G>A	XP_011510533.1:n.*646G>A
XM_011512232.1:c.*646G>A	XP_011510534.1:n.*646G>A
NM_014795.4:c.*646G>A MANE Select	NP_055610.1:n.*646G>A
NM_001171653.2:c.*646G>A	NP_001165124.1:n.*646G>A