Canonical Allele Identifier: CA2643991991

Gene: WNT4

Linked Data

• gnomAD v4: 1-22129978-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129984_22129985del , CM000663.2:g.22129984_22129985del	GRCh38
NC_000001.10:g.22456477_22456478del , CM000663.1:g.22456477_22456478del	GRCh37
NC_000001.9:g.22329064_22329065del	NCBI36
NG_008974.1:g.18047_18048del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.78-129_78-128del MANE Select	ENSP00000290167.5:n.78-129_78-128del
ENST00000290167.10:c.78-129_78-128del	ENSP00000290167.5:n.78-129_78-128del
ENST00000441048.1:c.-88-129_-88-128del	ENSP00000388925.1:n.-88-129_-88-128del
NM_030761.4:c.78-129_78-128del	NP_110388.2:n.78-129_78-128del
XM_011541597.1:c.144-129_144-128del	XP_011539899.1:n.144-129_144-128del
XM_011541598.1:c.-88-129_-88-128del	XP_011539900.1:n.-88-129_-88-128del
XM_011541599.1:c.144-129_144-128del	XP_011539901.1:n.144-129_144-128del
XM_011541597.2:c.144-129_144-128del	XP_011539899.1:n.144-129_144-128del
XM_011541598.2:c.-88-129_-88-128del	XP_011539900.1:n.-88-129_-88-128del
NM_030761.5:c.78-129_78-128del MANE Select	NP_110388.2:n.78-129_78-128del