Canonical Allele Identifier: CA350592246
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 559391
ClinVar RCV Id: RCV000677099
dbSNP Id: rs1553623389
gnomAD v4: 2-218893193-C-A
MyVariant Identifiers: chr2:g.219757915C>A (hg19) chr2:g.218893193C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893193C>A , CM000664.2:g.218893193C>A GRCh38
NC_000002.11:g.219757915C>A , CM000664.1:g.219757915C>A GRCh37
NC_000002.10:g.219466159C>A NCBI36
NG_012179.1:g.17661C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1176C>A MANE Select ENSP00000258411.3:p.Cys392Ter
ENST00000258411.7:c.1176C>A ENSP00000258411.3:p.Cys392Ter
NM_025216.2:c.1176C>A NP_079492.2:p.Cys392Ter
XM_011511928.1:c.1125C>A XP_011510230.1:p.Cys375Ter
XM_011511929.1:c.1080C>A XP_011510231.1:p.Cys360Ter
XM_011511930.1:c.796C>A XP_011510232.1:p.Pro266Thr
XM_011511929.2:c.1080C>A XP_011510231.1:p.Cys360Ter
NM_025216.3:c.1176C>A MANE Select NP_079492.2:p.Cys392Ter
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