Canonical Allele Identifier: CA1144230598

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129907_22129908delinsGG , CM000663.2:g.22129907_22129908delinsGG	GRCh38
NC_000001.10:g.22456400_22456401delinsGG , CM000663.1:g.22456400_22456401delinsGG	GRCh37
NC_000001.9:g.22328987_22328988delinsGG	NCBI36
NG_008974.1:g.18119_18120delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.78-57_78-56delinsCC MANE Select	ENSP00000290167.5:n.78-57_78-56delinsCC
ENST00000290167.10:c.78-57_78-56delinsCC	ENSP00000290167.5:n.78-57_78-56delinsCC
ENST00000441048.1:c.-88-57_-88-56delinsCC	ENSP00000388925.1:n.-88-57_-88-56delinsCC
NM_030761.4:c.78-57_78-56delinsCC	NP_110388.2:n.78-57_78-56delinsCC
XM_011541597.1:c.144-57_144-56delinsCC	XP_011539899.1:n.144-57_144-56delinsCC
XM_011541598.1:c.-88-57_-88-56delinsCC	XP_011539900.1:n.-88-57_-88-56delinsCC
XM_011541599.1:c.144-57_144-56delinsCC	XP_011539901.1:n.144-57_144-56delinsCC
XM_011541597.2:c.144-57_144-56delinsCC	XP_011539899.1:n.144-57_144-56delinsCC
XM_011541598.2:c.-88-57_-88-56delinsCC	XP_011539900.1:n.-88-57_-88-56delinsCC
NM_030761.5:c.78-57_78-56delinsCC MANE Select	NP_110388.2:n.78-57_78-56delinsCC