Canonical Allele Identifier: CA350592514
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 939057
ClinVar RCV Id: RCV001208383
dbSNP Id: rs1575235227
gnomAD v4: 2-218893216-G-C
MyVariant Identifiers: chr2:g.219757938G>C (hg19) chr2:g.218893216G>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1199G>C MANE Select ENSP00000258411.3:p.Cys400Ser
ENST00000258411.7:c.1199G>C ENSP00000258411.3:p.Cys400Ser
NM_025216.2:c.1199G>C NP_079492.2:p.Cys400Ser
XM_011511928.1:c.1148G>C XP_011510230.1:p.Cys383Ser
XM_011511929.1:c.1103G>C XP_011510231.1:p.Cys368Ser
XM_011511930.1:c.819G>C XP_011510232.1:p.Leu273=
XM_011511929.2:c.1103G>C XP_011510231.1:p.Cys368Ser
NM_025216.3:c.1199G>C MANE Select NP_079492.2:p.Cys400Ser
Search 100 bp 5'
Search 100 bp 3'