Canonical Allele Identifier: CA731858511

Gene: WNT4

Linked Data

• dbSNP Id: rs1166311693
• MyVariant Identifiers: chr1:g.22456294_22456300del (hg19) ; chr1:g.22129801_22129807del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129802_22129808del , CM000663.2:g.22129802_22129808del	GRCh38
NC_000001.10:g.22456295_22456301del , CM000663.1:g.22456295_22456301del	GRCh37
NC_000001.9:g.22328882_22328888del	NCBI36
NG_008974.1:g.18220_18226del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.122_128del MANE Select	ENSP00000290167.5:p.Glu41AlafsTer7
ENST00000290167.10:c.122_128del	ENSP00000290167.5:p.Glu41AlafsTer7
ENST00000415567.1:c.45_51del
ENST00000441048.1:c.-44_-38del	ENSP00000388925.1:n.-44_-38del
NM_030761.4:c.122_128del	NP_110388.2:p.Glu41AlafsTer7
XM_011541597.1:c.188_194del	XP_011539899.1:p.Glu63AlafsTer7
XM_011541598.1:c.-44_-38del	XP_011539900.1:n.-44_-38del
XM_011541599.1:c.188_194del	XP_011539901.1:p.Glu63AlafsTer7
XM_011541597.2:c.188_194del	XP_011539899.1:p.Glu63AlafsTer7
XM_011541598.2:c.-44_-38del	XP_011539900.1:n.-44_-38del
NM_030761.5:c.122_128del MANE Select	NP_110388.2:p.Glu41AlafsTer7