Canonical Allele Identifier: CA431234855
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893244-C-A
MyVariant Identifiers: chr2:g.219757966C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893244C>A , CM000664.2:g.218893244C>A GRCh38
NC_000002.11:g.219757966C>A , CM000664.1:g.219757966C>A GRCh37
NC_000002.10:g.219466210C>A NCBI36
NG_012179.1:g.17712C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1227C>A MANE Select ENSP00000258411.3:p.Ile409=
ENST00000258411.7:c.1227C>A ENSP00000258411.3:p.Ile409=
ENST00000489887.1:n.24C>A
NM_025216.2:c.1227C>A NP_079492.2:p.Ile409=
XM_011511928.1:c.1176C>A XP_011510230.1:p.Ile392=
XM_011511929.1:c.1131C>A XP_011510231.1:p.Ile377=
XM_011511930.1:c.847C>A XP_011510232.1:p.His283Asn
XM_011511929.2:c.1131C>A XP_011510231.1:p.Ile377=
NM_025216.3:c.1227C>A MANE Select NP_079492.2:p.Ile409=
Search 100 bp 5'
Search 100 bp 3'