Canonical Allele Identifier: CA338921304
Gene: WNT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22129760A>T , CM000663.2:g.22129760A>T GRCh38
NC_000001.10:g.22456253A>T , CM000663.1:g.22456253A>T GRCh37
NC_000001.9:g.22328840A>T NCBI36
NG_008974.1:g.18267T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290167.11:c.169T>A MANE Select ENSP00000290167.5:p.Cys57Ser
ENST00000290167.10:c.169T>A ENSP00000290167.5:p.Cys57Ser
ENST00000415567.1:c.92T>A
ENST00000441048.1:c.4T>A ENSP00000388925.1:p.Cys2Ser
NM_030761.4:c.169T>A NP_110388.2:p.Cys57Ser
XM_011541597.1:c.235T>A XP_011539899.1:p.Cys79Ser
XM_011541598.1:c.4T>A XP_011539900.1:p.Cys2Ser
XM_011541599.1:c.235T>A XP_011539901.1:p.Cys79Ser
XM_011541597.2:c.235T>A XP_011539899.1:p.Cys79Ser
XM_011541598.2:c.4T>A XP_011539900.1:p.Cys2Ser
NM_030761.5:c.169T>A MANE Select NP_110388.2:p.Cys57Ser