Canonical Allele Identifier: CA10614200
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 334417
ClinVar RCV Id: RCV000298619 RCV000343286 RCV000395886
dbSNP Id: rs190527122
gnomAD v2: 2-219758101-G-A
gnomAD v3: 2-218893379-G-A
gnomAD v4: 2-218893379-G-A
MyVariant Identifiers: chr2:g.219758101G>A (hg19) chr2:g.218893379G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893379G>A , CM000664.2:g.218893379G>A GRCh38
NC_000002.11:g.219758101G>A , CM000664.1:g.219758101G>A GRCh37
NC_000002.10:g.219466345G>A NCBI36
NG_012179.1:g.17847G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.*108G>A MANE Select ENSP00000258411.3:n.*108G>A
ENST00000258411.7:c.*108G>A ENSP00000258411.3:n.*108G>A
ENST00000489887.1:n.47+112G>A
NM_025216.2:c.*108G>A NP_079492.2:n.*108G>A
XM_011511928.1:c.*108G>A XP_011510230.1:n.*108G>A
XM_011511929.1:c.*108G>A XP_011510231.1:n.*108G>A
XM_011511930.1:c.*82G>A XP_011510232.1:n.*82G>A
XM_011511929.2:c.*108G>A XP_011510231.1:n.*108G>A
NM_025216.3:c.*108G>A MANE Select NP_079492.2:n.*108G>A
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