Canonical Allele Identifier: CA431234828
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1538167
ClinVar RCV Id: RCV002167148
dbSNP Id: rs1166558151
gnomAD v3: 2-218893187-G-A
gnomAD v4: 2-218893187-G-A
MyVariant Identifiers: chr2:g.219757909G>A (hg19) chr2:g.218893187G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893187G>A , CM000664.2:g.218893187G>A GRCh38
NC_000002.11:g.219757909G>A , CM000664.1:g.219757909G>A GRCh37
NC_000002.10:g.219466153G>A NCBI36
NG_012179.1:g.17655G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1170G>A MANE Select ENSP00000258411.3:p.Glu390=
ENST00000258411.7:c.1170G>A ENSP00000258411.3:p.Glu390=
NM_025216.2:c.1170G>A NP_079492.2:p.Glu390=
XM_011511928.1:c.1119G>A XP_011510230.1:p.Glu373=
XM_011511929.1:c.1074G>A XP_011510231.1:p.Glu358=
XM_011511930.1:c.790G>A XP_011510232.1:p.Ala264Thr
XM_011511929.2:c.1074G>A XP_011510231.1:p.Glu358=
NM_025216.3:c.1170G>A MANE Select NP_079492.2:p.Glu390=
Search 100 bp 5'
Search 100 bp 3'