Canonical Allele Identifier: CA675464

Gene: WNT4

Linked Data

• dbSNP Id: rs755587103
• ExAC: 1:22456078 T / TCGCCTGCAGCCCCGCACGCC
• gnomAD v2: 1-22456078-T-TCGCCTGCAGCCCCGCACGCC
• gnomAD v3: 1-22129585-T-TCGCCTGCAGCCCCGCACGCC
• gnomAD v4: 1-22129585-T-TCGCCTGCAGCCCCGCACGCC
• MyVariant Identifiers: chr1:g.22456078_22456079insCGCCTGCAGCCCCGCACGCC (hg19) ; chr1:g.22129585_22129586insCGCCTGCAGCCCCGCACGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129586_22129587insGCCTGCAGCCCCGCACGCCC , CM000663.2:g.22129586_22129587insGCCTGCAGCCCCGCACGCCC	GRCh38
NC_000001.10:g.22456079_22456080insGCCTGCAGCCCCGCACGCCC , CM000663.1:g.22456079_22456080insGCCTGCAGCCCCGCACGCCC	GRCh37
NC_000001.9:g.22328666_22328667insGCCTGCAGCCCCGCACGCCC	NCBI36
NG_008974.1:g.18441_18442insGGCGTGCGGGGCTGCAGGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.313+30_313+31insGGCGTGCGGGGCTGCAGGCG MANE Select	ENSP00000290167.5:n.313+30_313+31insGGCGTGCGGGGCTGCAGGCG
ENST00000290167.10:c.313+30_313+31insGGCGTGCGGGGCTGCAGGCG	ENSP00000290167.5:n.313+30_313+31insGGCGTGCGGGGCTGCAGGCG
ENST00000415567.1:c.236+30_236+31insGGCGTGCGGGGCTGCAGGCG
ENST00000441048.1:c.148+30_148+31insGGCGTGCGGGGCTGCAGGCG	ENSP00000388925.1:n.148+30_148+31insGGCGTGCGGGGCTGCAGGCG
NM_030761.4:c.313+30_313+31insGGCGTGCGGGGCTGCAGGCG	NP_110388.2:n.313+30_313+31insGGCGTGCGGGGCTGCAGGCG
XM_011541597.1:c.379+30_379+31insGGCGTGCGGGGCTGCAGGCG	XP_011539899.1:n.379+30_379+31insGGCGTGCGGGGCTGCAGGCG
XM_011541598.1:c.148+30_148+31insGGCGTGCGGGGCTGCAGGCG	XP_011539900.1:n.148+30_148+31insGGCGTGCGGGGCTGCAGGCG
XM_011541599.1:c.379+30_379+31insGGCGTGCGGGGCTGCAGGCG	XP_011539901.1:n.379+30_379+31insGGCGTGCGGGGCTGCAGGCG
XM_011541597.2:c.379+30_379+31insGGCGTGCGGGGCTGCAGGCG	XP_011539899.1:n.379+30_379+31insGGCGTGCGGGGCTGCAGGCG
XM_011541598.2:c.148+30_148+31insGGCGTGCGGGGCTGCAGGCG	XP_011539900.1:n.148+30_148+31insGGCGTGCGGGGCTGCAGGCG
NM_030761.5:c.313+30_313+31insGGCGTGCGGGGCTGCAGGCG MANE Select	NP_110388.2:n.313+30_313+31insGGCGTGCGGGGCTGCAGGCG