Canonical Allele Identifier: CA431234837
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1953433
ClinVar RCV Id: RCV002700323
dbSNP Id: rs1326745283
gnomAD v2: 2-219757927-C-T
gnomAD v4: 2-218893205-C-T
MyVariant Identifiers: chr2:g.219757927C>T (hg19) chr2:g.218893205C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893205C>T , CM000664.2:g.218893205C>T GRCh38
NC_000002.11:g.219757927C>T , CM000664.1:g.219757927C>T GRCh37
NC_000002.10:g.219466171C>T NCBI36
NG_012179.1:g.17673C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1188C>T MANE Select ENSP00000258411.3:p.Phe396=
ENST00000258411.7:c.1188C>T ENSP00000258411.3:p.Phe396=
NM_025216.2:c.1188C>T NP_079492.2:p.Phe396=
XM_011511928.1:c.1137C>T XP_011510230.1:p.Phe379=
XM_011511929.1:c.1092C>T XP_011510231.1:p.Phe364=
XM_011511930.1:c.808C>T XP_011510232.1:p.Pro270Ser
XM_011511929.2:c.1092C>T XP_011510231.1:p.Phe364=
NM_025216.3:c.1188C>T MANE Select NP_079492.2:p.Phe396=
Search 100 bp 5'
Search 100 bp 3'