Canonical Allele Identifier: CA431416466
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2953943
ClinVar RCV Id: RCV003813166
dbSNP Id: rs1381185098
gnomAD v3: 2-218882266-G-A
gnomAD v4: 2-218882266-G-A
MyVariant Identifiers: chr2:g.219746988G>A (hg19) chr2:g.218882266G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882266G>A , CM000664.2:g.218882266G>A GRCh38
NC_000002.11:g.219746988G>A , CM000664.1:g.219746988G>A GRCh37
NC_000002.10:g.219455232G>A NCBI36
NG_012179.1:g.6734G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.219G>A MANE Select ENSP00000258411.3:p.Glu73=
ENST00000258411.7:c.219G>A ENSP00000258411.3:p.Glu73=
ENST00000458582.1:c.106G>A
NM_025216.2:c.219G>A NP_079492.2:p.Glu73=
XM_011511928.1:c.168G>A XP_011510230.1:p.Glu56=
XM_011511929.1:c.123G>A XP_011510231.1:p.Glu41=
XM_011511930.1:c.219G>A XP_011510232.1:p.Glu73=
XM_011511929.2:c.123G>A XP_011510231.1:p.Glu41=
NM_025216.3:c.219G>A MANE Select NP_079492.2:p.Glu73=
Search 100 bp 5'
Search 100 bp 3'