Canonical Allele Identifier: CA431416448
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1157813
ClinVar RCV Id: RCV001500983
dbSNP Id: rs1163565666
gnomAD v2: 2-219746959-T-C
MyVariant Identifiers: chr2:g.219746959T>C (hg19) chr2:g.218882237T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882237T>C , CM000664.2:g.218882237T>C GRCh38
NC_000002.11:g.219746959T>C , CM000664.1:g.219746959T>C GRCh37
NC_000002.10:g.219455203T>C NCBI36
NG_012179.1:g.6705T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.190T>C MANE Select ENSP00000258411.3:p.Leu64=
ENST00000258411.7:c.190T>C ENSP00000258411.3:p.Leu64=
ENST00000458582.1:c.77T>C
NM_025216.2:c.190T>C NP_079492.2:p.Leu64=
XM_011511928.1:c.139T>C XP_011510230.1:p.Leu47=
XM_011511929.1:c.94T>C XP_011510231.1:p.Leu32=
XM_011511930.1:c.190T>C XP_011510232.1:p.Leu64=
XM_011511929.2:c.94T>C XP_011510231.1:p.Leu32=
NM_025216.3:c.190T>C MANE Select NP_079492.2:p.Leu64=
Search 100 bp 5'
Search 100 bp 3'