Canonical Allele Identifier: CA348704011

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145154042C>G (hg19) ; chr2:g.144396475C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396475C>G , CM000664.2:g.144396475C>G	GRCh38
NC_000002.11:g.145154042C>G , CM000664.1:g.145154042C>G	GRCh37
NC_000002.10:g.144870512C>G	NCBI36
NG_016431.1:g.128917G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2853G>C	ENSP00000508434.1:n.*2853G>C
ENST00000440875.6:c.2227G>C	ENSP00000475553.3:p.Asp743His
ENST00000627532.3:c.3004G>C MANE Select	ENSP00000487174.1:p.Asp1002His
ENST00000636026.2:c.3004G>C	ENSP00000490776.1:p.Asp1002His
ENST00000636179.1:n.2973G>C
ENST00000636413.1:c.2668G>C	ENSP00000490508.1:p.Asp890His
ENST00000636471.1:c.3079G>C	ENSP00000490317.1:p.Asp1027His
ENST00000636732.2:c.*2721G>C	ENSP00000490175.1:n.*2721G>C
ENST00000636820.1:n.3104G>C
ENST00000637045.1:c.2668G>C	ENSP00000490141.1:p.Asp890His
ENST00000637304.1:c.2668G>C	ENSP00000490872.1:p.Asp890His
ENST00000638007.1:c.2668G>C	ENSP00000490723.1:p.Asp890His
ENST00000638087.1:c.2668G>C	ENSP00000490673.1:p.Asp890His
ENST00000638128.1:c.2227G>C	ENSP00000490934.1:p.Asp743His
ENST00000639389.1:c.88G>C	ENSP00000492572.1:p.Asp30His
ENST00000647488.1:c.136G>C	ENSP00000494820.1:p.Asp46His
ENST00000675069.1:c.535G>C	ENSP00000502467.1:p.Asp179His
ENST00000303660.8:c.3001G>C	ENSP00000302501.4:p.Asp1001His
ENST00000409487.7:c.3004G>C	ENSP00000386854.2:p.Asp1002His
ENST00000419938.5:c.655+4724G>C	ENSP00000394777.2:n.655+4724G>C
ENST00000539609.7:c.2932G>C	ENSP00000443792.2:p.Asp978His
ENST00000558170.6:c.3004G>C	ENSP00000454157.1:p.Asp1002His
ENST00000627532.2:c.3004G>C	ENSP00000487174.1:p.Asp1002His
NM_001171653.1:c.2932G>C	NP_001165124.1:p.Asp978His
NM_014795.3:c.3004G>C	NP_055610.1:p.Asp1002His
XM_006712881.2:c.3004G>C	XP_006712944.1:p.Asp1002His
XM_006712882.2:c.3004G>C	XP_006712945.1:p.Asp1002His
XM_011512231.1:c.2995G>C	XP_011510533.1:p.Asp999His
XM_011512232.1:c.2983G>C	XP_011510534.1:p.Asp995His
NM_014795.4:c.3004G>C MANE Select	NP_055610.1:p.Asp1002His
NM_001171653.2:c.2932G>C	NP_001165124.1:p.Asp978His