Canonical Allele Identifier: CA338921613

Gene: WNT4

Linked Data

• gnomAD v4: 1-22129808-C-T
• MyVariant Identifiers: chr1:g.22456301C>T (hg19) ; chr1:g.22129808C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129808C>T , CM000663.2:g.22129808C>T	GRCh38
NC_000001.10:g.22456301C>T , CM000663.1:g.22456301C>T	GRCh37
NC_000001.9:g.22328888C>T	NCBI36
NG_008974.1:g.18219G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.121G>A MANE Select	ENSP00000290167.5:p.Glu41Lys
ENST00000290167.10:c.121G>A	ENSP00000290167.5:p.Glu41Lys
ENST00000415567.1:c.44G>A
ENST00000441048.1:c.-45G>A	ENSP00000388925.1:n.-45G>A
NM_030761.4:c.121G>A	NP_110388.2:p.Glu41Lys
XM_011541597.1:c.187G>A	XP_011539899.1:p.Glu63Lys
XM_011541598.1:c.-45G>A	XP_011539900.1:n.-45G>A
XM_011541599.1:c.187G>A	XP_011539901.1:p.Glu63Lys
XM_011541597.2:c.187G>A	XP_011539899.1:p.Glu63Lys
XM_011541598.2:c.-45G>A	XP_011539900.1:n.-45G>A
NM_030761.5:c.121G>A MANE Select	NP_110388.2:p.Glu41Lys