Canonical Allele Identifier: CA338921839

Gene: WNT4

Linked Data

• gnomAD v4: 1-22129844-C-T
• COSMIC: COSM1560256 ; COSM1560257
• MyVariant Identifiers: chr1:g.22456337C>T (hg19) ; chr1:g.22129844C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129844C>T , CM000663.2:g.22129844C>T	GRCh38
NC_000001.10:g.22456337C>T , CM000663.1:g.22456337C>T	GRCh37
NC_000001.9:g.22328924C>T	NCBI36
NG_008974.1:g.18183G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.85G>A MANE Select	ENSP00000290167.5:p.Ala29Thr
ENST00000290167.10:c.85G>A	ENSP00000290167.5:p.Ala29Thr
ENST00000415567.1:c.8G>A
ENST00000441048.1:c.-81G>A	ENSP00000388925.1:n.-81G>A
NM_030761.4:c.85G>A	NP_110388.2:p.Ala29Thr
XM_011541597.1:c.151G>A	XP_011539899.1:p.Ala51Thr
XM_011541598.1:c.-81G>A	XP_011539900.1:n.-81G>A
XM_011541599.1:c.151G>A	XP_011539901.1:p.Ala51Thr
XM_011541597.2:c.151G>A	XP_011539899.1:p.Ala51Thr
XM_011541598.2:c.-81G>A	XP_011539900.1:n.-81G>A
NM_030761.5:c.85G>A MANE Select	NP_110388.2:p.Ala29Thr