Canonical Allele Identifier: CA350592511
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 807721
ClinVar RCV Id: RCV000995914
dbSNP Id: rs1575235227
gnomAD v4: 2-218893216-G-A
MyVariant Identifiers: chr2:g.219757938G>A (hg19) chr2:g.218893216G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893216G>A , CM000664.2:g.218893216G>A GRCh38
NC_000002.11:g.219757938G>A , CM000664.1:g.219757938G>A GRCh37
NC_000002.10:g.219466182G>A NCBI36
NG_012179.1:g.17684G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1199G>A MANE Select ENSP00000258411.3:p.Cys400Tyr
ENST00000258411.7:c.1199G>A ENSP00000258411.3:p.Cys400Tyr
NM_025216.2:c.1199G>A NP_079492.2:p.Cys400Tyr
XM_011511928.1:c.1148G>A XP_011510230.1:p.Cys383Tyr
XM_011511929.1:c.1103G>A XP_011510231.1:p.Cys368Tyr
XM_011511930.1:c.819G>A XP_011510232.1:p.Leu273=
XM_011511929.2:c.1103G>A XP_011510231.1:p.Cys368Tyr
NM_025216.3:c.1199G>A MANE Select NP_079492.2:p.Cys400Tyr
Search 100 bp 5'
Search 100 bp 3'