Canonical Allele Identifier: CA338921476
Gene: WNT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22129788C>A , CM000663.2:g.22129788C>A GRCh38
NC_000001.10:g.22456281C>A , CM000663.1:g.22456281C>A GRCh37
NC_000001.9:g.22328868C>A NCBI36
NG_008974.1:g.18239G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000290167.11:c.141G>T MANE Select ENSP00000290167.5:p.Lys47Asn
ENST00000290167.10:c.141G>T ENSP00000290167.5:p.Lys47Asn
ENST00000415567.1:c.64G>T
ENST00000441048.1:c.-25G>T ENSP00000388925.1:n.-25G>T
NM_030761.4:c.141G>T NP_110388.2:p.Lys47Asn
XM_011541597.1:c.207G>T XP_011539899.1:p.Lys69Asn
XM_011541598.1:c.-25G>T XP_011539900.1:n.-25G>T
XM_011541599.1:c.207G>T XP_011539901.1:p.Lys69Asn
XM_011541597.2:c.207G>T XP_011539899.1:p.Lys69Asn
XM_011541598.2:c.-25G>T XP_011539900.1:n.-25G>T
NM_030761.5:c.141G>T MANE Select NP_110388.2:p.Lys47Asn