Canonical Allele Identifier: CA2643991885
Gene: WNT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22129897del , CM000663.2:g.22129897del GRCh38
NC_000001.10:g.22456390del , CM000663.1:g.22456390del GRCh37
NC_000001.9:g.22328977del NCBI36
NG_008974.1:g.18132del

Transcript Alleles

HGVS Amino-acid Change
ENST00000290167.11:c.78-44del MANE Select ENSP00000290167.5:n.78-44del
ENST00000290167.10:c.78-44del ENSP00000290167.5:n.78-44del
ENST00000441048.1:c.-88-44del ENSP00000388925.1:n.-88-44del
NM_030761.4:c.78-44del NP_110388.2:n.78-44del
XM_011541597.1:c.144-44del XP_011539899.1:n.144-44del
XM_011541598.1:c.-88-44del XP_011539900.1:n.-88-44del
XM_011541599.1:c.144-44del XP_011539901.1:n.144-44del
XM_011541597.2:c.144-44del XP_011539899.1:n.144-44del
XM_011541598.2:c.-88-44del XP_011539900.1:n.-88-44del
NM_030761.5:c.78-44del MANE Select NP_110388.2:n.78-44del