Canonical Allele Identifier: CA338921562

Gene: WNT4

Linked Data

• dbSNP Id: rs148427888
• gnomAD v2: 1-22456293-G-T
• gnomAD v4: 1-22129800-G-T
• MyVariant Identifiers: chr1:g.22456293G>T (hg19) ; chr1:g.22129800G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129800G>T , CM000663.2:g.22129800G>T	GRCh38
NC_000001.10:g.22456293G>T , CM000663.1:g.22456293G>T	GRCh37
NC_000001.9:g.22328880G>T	NCBI36
NG_008974.1:g.18227C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.129C>A MANE Select	ENSP00000290167.5:p.Cys43Ter
ENST00000290167.10:c.129C>A	ENSP00000290167.5:p.Cys43Ter
ENST00000415567.1:c.52C>A
ENST00000441048.1:c.-37C>A	ENSP00000388925.1:n.-37C>A
NM_030761.4:c.129C>A	NP_110388.2:p.Cys43Ter
XM_011541597.1:c.195C>A	XP_011539899.1:p.Cys65Ter
XM_011541598.1:c.-37C>A	XP_011539900.1:n.-37C>A
XM_011541599.1:c.195C>A	XP_011539901.1:p.Cys65Ter
XM_011541597.2:c.195C>A	XP_011539899.1:p.Cys65Ter
XM_011541598.2:c.-37C>A	XP_011539900.1:n.-37C>A
NM_030761.5:c.129C>A MANE Select	NP_110388.2:p.Cys43Ter