Canonical Allele Identifier: CA431234861
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1674226
ClinVar RCV Id: RCV002206515
dbSNP Id: rs1189350015
gnomAD v2: 2-219757978-C-A
gnomAD v3: 2-218893256-C-A
gnomAD v4: 2-218893256-C-A
MyVariant Identifiers: chr2:g.219757978C>A (hg19) chr2:g.218893256C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893256C>A , CM000664.2:g.218893256C>A GRCh38
NC_000002.11:g.219757978C>A , CM000664.1:g.219757978C>A GRCh37
NC_000002.10:g.219466222C>A NCBI36
NG_012179.1:g.17724C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1239C>A MANE Select ENSP00000258411.3:p.Val413=
ENST00000258411.7:c.1239C>A ENSP00000258411.3:p.Val413=
ENST00000489887.1:n.36C>A
NM_025216.2:c.1239C>A NP_079492.2:p.Val413=
XM_011511928.1:c.1188C>A XP_011510230.1:p.Val396=
XM_011511929.1:c.1143C>A XP_011510231.1:p.Val381=
XM_011511930.1:c.859C>A XP_011510232.1:p.Gln287Lys
XM_011511929.2:c.1143C>A XP_011510231.1:p.Val381=
NM_025216.3:c.1239C>A MANE Select NP_079492.2:p.Val413=
Search 100 bp 5'
Search 100 bp 3'