Canonical Allele Identifier: CA348705066

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145154160C>G (hg19) ; chr2:g.144396593C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396593C>G , CM000664.2:g.144396593C>G	GRCh38
NC_000002.11:g.145154160C>G , CM000664.1:g.145154160C>G	GRCh37
NC_000002.10:g.144870630C>G	NCBI36
NG_016431.1:g.128799G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2736-1G>C	ENSP00000508434.1:n.*2736-1G>C
ENST00000440875.6:c.2110-1G>C	ENSP00000475553.3:n.2110-1G>C
ENST00000627532.3:c.2887-1G>C MANE Select	ENSP00000487174.1:n.2887-1G>C
ENST00000636026.2:c.2887-1G>C	ENSP00000490776.1:n.2887-1G>C
ENST00000636179.1:n.2856-1G>C
ENST00000636413.1:c.2551-1G>C	ENSP00000490508.1:n.2551-1G>C
ENST00000636471.1:c.2962-1G>C	ENSP00000490317.1:n.2962-1G>C
ENST00000636732.2:c.*2604-1G>C	ENSP00000490175.1:n.*2604-1G>C
ENST00000636820.1:n.2987-1G>C
ENST00000637045.1:c.2551-1G>C	ENSP00000490141.1:n.2551-1G>C
ENST00000637304.1:c.2551-1G>C	ENSP00000490872.1:n.2551-1G>C
ENST00000638007.1:c.2551-1G>C	ENSP00000490723.1:n.2551-1G>C
ENST00000638087.1:c.2551-1G>C	ENSP00000490673.1:n.2551-1G>C
ENST00000638128.1:c.2110-1G>C	ENSP00000490934.1:n.2110-1G>C
ENST00000647488.1:c.19-1G>C	ENSP00000494820.1:n.19-1G>C
ENST00000675069.1:c.418-1G>C	ENSP00000502467.1:n.418-1G>C
ENST00000303660.8:c.2884-1G>C	ENSP00000302501.4:n.2884-1G>C
ENST00000409487.7:c.2887-1G>C	ENSP00000386854.2:n.2887-1G>C
ENST00000419938.5:c.655+4606G>C	ENSP00000394777.2:n.655+4606G>C
ENST00000539609.7:c.2815-1G>C	ENSP00000443792.2:n.2815-1G>C
ENST00000558170.6:c.2887-1G>C	ENSP00000454157.1:n.2887-1G>C
ENST00000627532.2:c.2887-1G>C	ENSP00000487174.1:n.2887-1G>C
NM_001171653.1:c.2815-1G>C	NP_001165124.1:n.2815-1G>C
NM_014795.3:c.2887-1G>C	NP_055610.1:n.2887-1G>C
XM_006712881.2:c.2887-1G>C	XP_006712944.1:n.2887-1G>C
XM_006712882.2:c.2887-1G>C	XP_006712945.1:n.2887-1G>C
XM_011512231.1:c.2878-1G>C	XP_011510533.1:n.2878-1G>C
XM_011512232.1:c.2866-1G>C	XP_011510534.1:n.2866-1G>C
NM_014795.4:c.2887-1G>C MANE Select	NP_055610.1:n.2887-1G>C
NM_001171653.2:c.2815-1G>C	NP_001165124.1:n.2815-1G>C