Canonical Allele Identifier: CA19150141

Gene: WNT4

Linked Data

• dbSNP Id: rs993354934
• gnomAD v3: 1-22129869-CG-C
• gnomAD v4: 1-22129869-CG-C
• MyVariant Identifiers: chr1:g.22456363del (hg19) ; chr1:g.22129870del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129870del , CM000663.2:g.22129870del	GRCh38
NC_000001.10:g.22456363del , CM000663.1:g.22456363del	GRCh37
NC_000001.9:g.22328950del	NCBI36
NG_008974.1:g.18157del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.78-19del MANE Select	ENSP00000290167.5:n.78-19del
ENST00000290167.10:c.78-19del	ENSP00000290167.5:n.78-19del
ENST00000441048.1:c.-88-19del	ENSP00000388925.1:n.-88-19del
NM_030761.4:c.78-19del	NP_110388.2:n.78-19del
XM_011541597.1:c.144-19del	XP_011539899.1:n.144-19del
XM_011541598.1:c.-88-19del	XP_011539900.1:n.-88-19del
XM_011541599.1:c.144-19del	XP_011539901.1:n.144-19del
XM_011541597.2:c.144-19del	XP_011539899.1:n.144-19del
XM_011541598.2:c.-88-19del	XP_011539900.1:n.-88-19del
NM_030761.5:c.78-19del MANE Select	NP_110388.2:n.78-19del