Canonical Allele Identifier: CA338921648

Gene: WNT4

Linked Data

• dbSNP Id: rs1157460274
• gnomAD v2: 1-22456306-T-C
• gnomAD v4: 1-22129813-T-C
• MyVariant Identifiers: chr1:g.22456306T>C (hg19) ; chr1:g.22129813T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129813T>C , CM000663.2:g.22129813T>C	GRCh38
NC_000001.10:g.22456306T>C , CM000663.1:g.22456306T>C	GRCh37
NC_000001.9:g.22328893T>C	NCBI36
NG_008974.1:g.18214A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.116A>G MANE Select	ENSP00000290167.5:p.Glu39Gly
ENST00000290167.10:c.116A>G	ENSP00000290167.5:p.Glu39Gly
ENST00000415567.1:c.39A>G
ENST00000441048.1:c.-50A>G	ENSP00000388925.1:n.-50A>G
NM_030761.4:c.116A>G	NP_110388.2:p.Glu39Gly
XM_011541597.1:c.182A>G	XP_011539899.1:p.Glu61Gly
XM_011541598.1:c.-50A>G	XP_011539900.1:n.-50A>G
XM_011541599.1:c.182A>G	XP_011539901.1:p.Glu61Gly
XM_011541597.2:c.182A>G	XP_011539899.1:p.Glu61Gly
XM_011541598.2:c.-50A>G	XP_011539900.1:n.-50A>G
NM_030761.5:c.116A>G MANE Select	NP_110388.2:p.Glu39Gly