Canonical Allele Identifier: CA675489

Gene: WNT4

Linked Data

• ClinVar Variation Id: 1971047
• ClinVar RCV Id: RCV002735727
• dbSNP Id: rs201024257
• ExAC: 1:22456184 A / G
• gnomAD v2: 1-22456184-A-G
• gnomAD v3: 1-22129691-A-G
• gnomAD v4: 1-22129691-A-G
• MyVariant Identifiers: chr1:g.22456184A>G (hg19) ; chr1:g.22129691A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129691A>G , CM000663.2:g.22129691A>G	GRCh38
NC_000001.10:g.22456184A>G , CM000663.1:g.22456184A>G	GRCh37
NC_000001.9:g.22328771A>G	NCBI36
NG_008974.1:g.18336T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000290167.11:c.238T>C MANE Select	ENSP00000290167.5:p.Tyr80His
ENST00000290167.10:c.238T>C	ENSP00000290167.5:p.Tyr80His
ENST00000415567.1:c.161T>C
ENST00000441048.1:c.73T>C	ENSP00000388925.1:p.Tyr25His
NM_030761.4:c.238T>C	NP_110388.2:p.Tyr80His
XM_011541597.1:c.304T>C	XP_011539899.1:p.Tyr102His
XM_011541598.1:c.73T>C	XP_011539900.1:p.Tyr25His
XM_011541599.1:c.304T>C	XP_011539901.1:p.Tyr102His
XM_011541597.2:c.304T>C	XP_011539899.1:p.Tyr102His
XM_011541598.2:c.73T>C	XP_011539900.1:p.Tyr25His
NM_030761.5:c.238T>C MANE Select	NP_110388.2:p.Tyr80His