Canonical Allele Identifier: CA338920808
Gene: WNT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22129685A>C , CM000663.2:g.22129685A>C GRCh38
NC_000001.10:g.22456178A>C , CM000663.1:g.22456178A>C GRCh37
NC_000001.9:g.22328765A>C NCBI36
NG_008974.1:g.18342T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000290167.11:c.244T>G MANE Select ENSP00000290167.5:p.Phe82Val
ENST00000290167.10:c.244T>G ENSP00000290167.5:p.Phe82Val
ENST00000415567.1:c.167T>G
ENST00000441048.1:c.79T>G ENSP00000388925.1:p.Phe27Val
NM_030761.4:c.244T>G NP_110388.2:p.Phe82Val
XM_011541597.1:c.310T>G XP_011539899.1:p.Phe104Val
XM_011541598.1:c.79T>G XP_011539900.1:p.Phe27Val
XM_011541599.1:c.310T>G XP_011539901.1:p.Phe104Val
XM_011541597.2:c.310T>G XP_011539899.1:p.Phe104Val
XM_011541598.2:c.79T>G XP_011539900.1:p.Phe27Val
NM_030761.5:c.244T>G MANE Select NP_110388.2:p.Phe82Val