Canonical Allele Identifier: CA338920912

Gene: WNT4

Linked Data

• gnomAD v4: 1-22129695-G-T
• MyVariant Identifiers: chr1:g.22456188G>T (hg19) ; chr1:g.22129695G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129695G>T , CM000663.2:g.22129695G>T	GRCh38
NC_000001.10:g.22456188G>T , CM000663.1:g.22456188G>T	GRCh37
NC_000001.9:g.22328775G>T	NCBI36
NG_008974.1:g.18332C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000290167.11:c.234C>A MANE Select	ENSP00000290167.5:p.Cys78Ter
ENST00000290167.10:c.234C>A	ENSP00000290167.5:p.Cys78Ter
ENST00000415567.1:c.157C>A
ENST00000441048.1:c.69C>A	ENSP00000388925.1:p.Cys23Ter
NM_030761.4:c.234C>A	NP_110388.2:p.Cys78Ter
XM_011541597.1:c.300C>A	XP_011539899.1:p.Cys100Ter
XM_011541598.1:c.69C>A	XP_011539900.1:p.Cys23Ter
XM_011541599.1:c.300C>A	XP_011539901.1:p.Cys100Ter
XM_011541597.2:c.300C>A	XP_011539899.1:p.Cys100Ter
XM_011541598.2:c.69C>A	XP_011539900.1:p.Cys23Ter
NM_030761.5:c.234C>A MANE Select	NP_110388.2:p.Cys78Ter