Canonical Allele Identifier: CA1158260846
Gene: WNT4 HGNC NCBI

Linked Data

dbSNP Id: rs1645969260

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22129821_22129823dup , CM000663.2:g.22129821_22129823dup GRCh38
NC_000001.10:g.22456314_22456316dup , CM000663.1:g.22456314_22456316dup GRCh37
NC_000001.9:g.22328901_22328903dup NCBI36
NG_008974.1:g.18205_18207dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000290167.11:c.107_109dup MANE Select ENSP00000290167.5:p.Ser36_Ile37insSer
ENST00000290167.10:c.107_109dup ENSP00000290167.5:p.Ser36_Ile37insSer
ENST00000415567.1:c.30_32dup
ENST00000441048.1:c.-59_-57dup ENSP00000388925.1:n.-59_-57dup
NM_030761.4:c.107_109dup NP_110388.2:p.Ser36_Ile37insSer
XM_011541597.1:c.173_175dup XP_011539899.1:p.Ser58_Ile59insSer
XM_011541598.1:c.-59_-57dup XP_011539900.1:n.-59_-57dup
XM_011541599.1:c.173_175dup XP_011539901.1:p.Ser58_Ile59insSer
XM_011541597.2:c.173_175dup XP_011539899.1:p.Ser58_Ile59insSer
XM_011541598.2:c.-59_-57dup XP_011539900.1:n.-59_-57dup
NM_030761.5:c.107_109dup MANE Select NP_110388.2:p.Ser36_Ile37insSer