Canonical Allele Identifier: CA2114108
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 334414
ClinVar RCV Id: RCV000288484 RCV000333165 RCV000387692 RCV000414053 RCV000845114 RCV001082463 RCV002248620
dbSNP Id: rs34972707
ExAC: 2:219757826 A / C
gnomAD v2: 2-219757826-A-C
gnomAD v3: 2-218893104-A-C
gnomAD v4: 2-218893104-A-C
MyVariant Identifiers: chr2:g.219757826A>C (hg19) chr2:g.218893104A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893104A>C , CM000664.2:g.218893104A>C GRCh38
NC_000002.11:g.219757826A>C , CM000664.1:g.219757826A>C GRCh37
NC_000002.10:g.219466070A>C NCBI36
NG_012179.1:g.17572A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1087A>C MANE Select ENSP00000258411.3:p.Asn363His
ENST00000258411.7:c.1087A>C ENSP00000258411.3:p.Asn363His
ENST00000458582.1:c.594A>C
NM_025216.2:c.1087A>C NP_079492.2:p.Asn363His
XM_011511928.1:c.1036A>C XP_011510230.1:p.Asn346His
XM_011511929.1:c.991A>C XP_011510231.1:p.Asn331His
XM_011511930.1:c.707A>C XP_011510232.1:p.Gln236Pro
XM_011511929.2:c.991A>C XP_011510231.1:p.Asn331His
NM_025216.3:c.1087A>C MANE Select NP_079492.2:p.Asn363His
Search 100 bp 5'
Search 100 bp 3'