Canonical Allele Identifier: CA675512

Gene: WNT4

Linked Data

• dbSNP Id: rs747875232
• ExAC: 1:22456305 C / A
• gnomAD v2: 1-22456305-C-A
• gnomAD v3: 1-22129812-C-A
• gnomAD v4: 1-22129812-C-A
• MyVariant Identifiers: chr1:g.22456305C>A (hg19) ; chr1:g.22129812C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129812C>A , CM000663.2:g.22129812C>A	GRCh38
NC_000001.10:g.22456305C>A , CM000663.1:g.22456305C>A	GRCh37
NC_000001.9:g.22328892C>A	NCBI36
NG_008974.1:g.18215G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.117G>T MANE Select	ENSP00000290167.5:p.Glu39Asp
ENST00000290167.10:c.117G>T	ENSP00000290167.5:p.Glu39Asp
ENST00000415567.1:c.40G>T
ENST00000441048.1:c.-49G>T	ENSP00000388925.1:n.-49G>T
NM_030761.4:c.117G>T	NP_110388.2:p.Glu39Asp
XM_011541597.1:c.183G>T	XP_011539899.1:p.Glu61Asp
XM_011541598.1:c.-49G>T	XP_011539900.1:n.-49G>T
XM_011541599.1:c.183G>T	XP_011539901.1:p.Glu61Asp
XM_011541597.2:c.183G>T	XP_011539899.1:p.Glu61Asp
XM_011541598.2:c.-49G>T	XP_011539900.1:n.-49G>T
NM_030761.5:c.117G>T MANE Select	NP_110388.2:p.Glu39Asp