Canonical Allele Identifier: CA348699666

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145147339C>G (hg19) ; chr2:g.144389772C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389772C>G , CM000664.2:g.144389772C>G	GRCh38
NC_000002.11:g.145147339C>G , CM000664.1:g.145147339C>G	GRCh37
NC_000002.10:g.144863809C>G	NCBI36
NG_016431.1:g.135620G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3173G>C	ENSP00000508434.1:n.*3173G>C
ENST00000440875.6:c.2547G>C	ENSP00000475553.3:p.Met849Ile
ENST00000627532.3:c.3324G>C MANE Select	ENSP00000487174.1:p.Met1108Ile
ENST00000636026.2:c.3231-19G>C	ENSP00000490776.1:n.3231-19G>C
ENST00000636179.1:n.3293G>C
ENST00000636413.1:c.2988G>C	ENSP00000490508.1:p.Met996Ile
ENST00000636471.1:c.3399G>C	ENSP00000490317.1:p.Met1133Ile
ENST00000636732.2:c.*3041G>C	ENSP00000490175.1:n.*3041G>C
ENST00000636820.1:n.3424G>C
ENST00000637045.1:c.2988G>C	ENSP00000490141.1:p.Met996Ile
ENST00000637304.1:c.2988G>C	ENSP00000490872.1:p.Met996Ile
ENST00000638007.1:c.2988G>C	ENSP00000490723.1:p.Met996Ile
ENST00000638087.1:c.2988G>C	ENSP00000490673.1:p.Met996Ile
ENST00000638128.1:c.2547G>C	ENSP00000490934.1:p.Met849Ile
ENST00000639389.1:c.151+6640G>C	ENSP00000492572.1:n.151+6640G>C
ENST00000647488.1:c.544G>C	ENSP00000494820.1:n.544G>C
ENST00000675069.1:c.855G>C	ENSP00000502467.1:p.Met285Ile
ENST00000303660.8:c.3321G>C	ENSP00000302501.4:p.Met1107Ile
ENST00000409487.7:c.3324G>C	ENSP00000386854.2:p.Met1108Ile
ENST00000419938.5:c.656-890G>C	ENSP00000394777.2:n.656-890G>C
ENST00000539609.7:c.3252G>C	ENSP00000443792.2:p.Met1084Ile
ENST00000558170.6:c.3324G>C	ENSP00000454157.1:p.Met1108Ile
ENST00000627532.2:c.3324G>C	ENSP00000487174.1:p.Met1108Ile
NM_001171653.1:c.3252G>C	NP_001165124.1:p.Met1084Ile
NM_014795.3:c.3324G>C	NP_055610.1:p.Met1108Ile
XM_006712881.2:c.3324G>C	XP_006712944.1:p.Met1108Ile
XM_006712882.2:c.3324G>C	XP_006712945.1:p.Met1108Ile
XM_011512231.1:c.3315G>C	XP_011510533.1:p.Met1105Ile
XM_011512232.1:c.3303G>C	XP_011510534.1:p.Met1101Ile
NM_014795.4:c.3324G>C MANE Select	NP_055610.1:p.Met1108Ile
NM_001171653.2:c.3252G>C	NP_001165124.1:p.Met1084Ile