Canonical Allele Identifier: CA2742784996
Gene: WNT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22129966_22129967insGGATCATCCTCC , CM000663.2:g.22129966_22129967insGGATCATCCTCC GRCh38
NC_000001.10:g.22456459_22456460insGGATCATCCTCC , CM000663.1:g.22456459_22456460insGGATCATCCTCC GRCh37
NC_000001.9:g.22329046_22329047insGGATCATCCTCC NCBI36
NG_008974.1:g.18062_18063insAGGATGATCCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000290167.11:c.78-114_78-113insAGGATGATCCGG MANE Select ENSP00000290167.5:n.78-114_78-113insAGGATGATCCGG
ENST00000290167.10:c.78-114_78-113insAGGATGATCCGG ENSP00000290167.5:n.78-114_78-113insAGGATGATCCGG
ENST00000441048.1:c.-88-114_-88-113insAGGATGATCCGG ENSP00000388925.1:n.-88-114_-88-113insAGGATGATCCGG
NM_030761.4:c.78-114_78-113insAGGATGATCCGG NP_110388.2:n.78-114_78-113insAGGATGATCCGG
XM_011541597.1:c.144-114_144-113insAGGATGATCCGG XP_011539899.1:n.144-114_144-113insAGGATGATCCGG
XM_011541598.1:c.-88-114_-88-113insAGGATGATCCGG XP_011539900.1:n.-88-114_-88-113insAGGATGATCCGG
XM_011541599.1:c.144-114_144-113insAGGATGATCCGG XP_011539901.1:n.144-114_144-113insAGGATGATCCGG
XM_011541597.2:c.144-114_144-113insAGGATGATCCGG XP_011539899.1:n.144-114_144-113insAGGATGATCCGG
XM_011541598.2:c.-88-114_-88-113insAGGATGATCCGG XP_011539900.1:n.-88-114_-88-113insAGGATGATCCGG
NM_030761.5:c.78-114_78-113insAGGATGATCCGG MANE Select NP_110388.2:n.78-114_78-113insAGGATGATCCGG