Canonical Allele Identifier: CA338921877

Gene: WNT4

Linked Data

• dbSNP Id: rs1645969695
• MyVariant Identifiers: chr1:g.22456345C>T (hg19) ; chr1:g.22129852C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129852C>T , CM000663.2:g.22129852C>T	GRCh38
NC_000001.10:g.22456345C>T , CM000663.1:g.22456345C>T	GRCh37
NC_000001.9:g.22328932C>T	NCBI36
NG_008974.1:g.18175G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.78-1G>A MANE Select	ENSP00000290167.5:n.78-1G>A
ENST00000290167.10:c.78-1G>A	ENSP00000290167.5:n.78-1G>A
ENST00000441048.1:c.-88-1G>A	ENSP00000388925.1:n.-88-1G>A
NM_030761.4:c.78-1G>A	NP_110388.2:n.78-1G>A
XM_011541597.1:c.144-1G>A	XP_011539899.1:n.144-1G>A
XM_011541598.1:c.-88-1G>A	XP_011539900.1:n.-88-1G>A
XM_011541599.1:c.144-1G>A	XP_011539901.1:n.144-1G>A
XM_011541597.2:c.144-1G>A	XP_011539899.1:n.144-1G>A
XM_011541598.2:c.-88-1G>A	XP_011539900.1:n.-88-1G>A
NM_030761.5:c.78-1G>A MANE Select	NP_110388.2:n.78-1G>A