Canonical Allele Identifier: CA350592627
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 464179
ClinVar RCV Id: RCV000537520
dbSNP Id: rs1553623396
gnomAD v4: 2-218893229-C-G
MyVariant Identifiers: chr2:g.219757951C>G (hg19) chr2:g.218893229C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893229C>G , CM000664.2:g.218893229C>G GRCh38
NC_000002.11:g.219757951C>G , CM000664.1:g.219757951C>G GRCh37
NC_000002.10:g.219466195C>G NCBI36
NG_012179.1:g.17697C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1212C>G MANE Select ENSP00000258411.3:p.Cys404Trp
ENST00000258411.7:c.1212C>G ENSP00000258411.3:p.Cys404Trp
ENST00000489887.1:n.9C>G
NM_025216.2:c.1212C>G NP_079492.2:p.Cys404Trp
XM_011511928.1:c.1161C>G XP_011510230.1:p.Cys387Trp
XM_011511929.1:c.1116C>G XP_011510231.1:p.Cys372Trp
XM_011511930.1:c.832C>G XP_011510232.1:p.Arg278Gly
XM_011511929.2:c.1116C>G XP_011510231.1:p.Cys372Trp
NM_025216.3:c.1212C>G MANE Select NP_079492.2:p.Cys404Trp
Search 100 bp 5'
Search 100 bp 3'