Canonical Allele Identifier: CA1158260895
Gene: WNT4 HGNC NCBI

Linked Data

dbSNP Id: rs1645970401
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22129920_22129921insGCCTGAA , CM000663.2:g.22129920_22129921insGCCTGAA GRCh38
NC_000001.10:g.22456413_22456414insGCCTGAA , CM000663.1:g.22456413_22456414insGCCTGAA GRCh37
NC_000001.9:g.22329000_22329001insGCCTGAA NCBI36
NG_008974.1:g.18106_18107insTTCAGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000290167.11:c.78-70_78-69insTTCAGGC MANE Select ENSP00000290167.5:n.78-70_78-69insTTCAGGC
ENST00000290167.10:c.78-70_78-69insTTCAGGC ENSP00000290167.5:n.78-70_78-69insTTCAGGC
ENST00000441048.1:c.-88-70_-88-69insTTCAGGC ENSP00000388925.1:n.-88-70_-88-69insTTCAGGC
NM_030761.4:c.78-70_78-69insTTCAGGC NP_110388.2:n.78-70_78-69insTTCAGGC
XM_011541597.1:c.144-70_144-69insTTCAGGC XP_011539899.1:n.144-70_144-69insTTCAGGC
XM_011541598.1:c.-88-70_-88-69insTTCAGGC XP_011539900.1:n.-88-70_-88-69insTTCAGGC
XM_011541599.1:c.144-70_144-69insTTCAGGC XP_011539901.1:n.144-70_144-69insTTCAGGC
XM_011541597.2:c.144-70_144-69insTTCAGGC XP_011539899.1:n.144-70_144-69insTTCAGGC
XM_011541598.2:c.-88-70_-88-69insTTCAGGC XP_011539900.1:n.-88-70_-88-69insTTCAGGC
NM_030761.5:c.78-70_78-69insTTCAGGC MANE Select NP_110388.2:n.78-70_78-69insTTCAGGC
Search 100 bp 5'
Search 100 bp 3'