Canonical Allele Identifier: CA431417572
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1134514
ClinVar RCV Id: RCV001469473
dbSNP Id: rs1464589833
gnomAD v2: 2-219757900-G-A
gnomAD v4: 2-218893178-G-A
MyVariant Identifiers: chr2:g.219757900G>A (hg19) chr2:g.218893178G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893178G>A , CM000664.2:g.218893178G>A GRCh38
NC_000002.11:g.219757900G>A , CM000664.1:g.219757900G>A GRCh37
NC_000002.10:g.219466144G>A NCBI36
NG_012179.1:g.17646G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1161G>A MANE Select ENSP00000258411.3:p.Thr387=
ENST00000258411.7:c.1161G>A ENSP00000258411.3:p.Thr387=
NM_025216.2:c.1161G>A NP_079492.2:p.Thr387=
XM_011511928.1:c.1110G>A XP_011510230.1:p.Thr370=
XM_011511929.1:c.1065G>A XP_011510231.1:p.Thr355=
XM_011511930.1:c.781G>A XP_011510232.1:p.Ala261Thr
XM_011511929.2:c.1065G>A XP_011510231.1:p.Thr355=
NM_025216.3:c.1161G>A MANE Select NP_079492.2:p.Thr387=
Search 100 bp 5'
Search 100 bp 3'