Canonical Allele Identifier: CA521901595

Gene: WNT4

Linked Data

• dbSNP Id: rs1363859508
• gnomAD v2: 1-22456391-C-T
• gnomAD v3: 1-22129898-C-T
• gnomAD v4: 1-22129898-C-T
• MyVariant Identifiers: chr1:g.22456391C>T (hg19) ; chr1:g.22129898C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129898C>T , CM000663.2:g.22129898C>T	GRCh38
NC_000001.10:g.22456391C>T , CM000663.1:g.22456391C>T	GRCh37
NC_000001.9:g.22328978C>T	NCBI36
NG_008974.1:g.18129G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.78-47G>A MANE Select	ENSP00000290167.5:n.78-47G>A
ENST00000290167.10:c.78-47G>A	ENSP00000290167.5:n.78-47G>A
ENST00000441048.1:c.-88-47G>A	ENSP00000388925.1:n.-88-47G>A
NM_030761.4:c.78-47G>A	NP_110388.2:n.78-47G>A
XM_011541597.1:c.144-47G>A	XP_011539899.1:n.144-47G>A
XM_011541598.1:c.-88-47G>A	XP_011539900.1:n.-88-47G>A
XM_011541599.1:c.144-47G>A	XP_011539901.1:n.144-47G>A
XM_011541597.2:c.144-47G>A	XP_011539899.1:n.144-47G>A
XM_011541598.2:c.-88-47G>A	XP_011539900.1:n.-88-47G>A
NM_030761.5:c.78-47G>A MANE Select	NP_110388.2:n.78-47G>A