Canonical Allele Identifier: CA431416431
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219746940C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882218C>A , CM000664.2:g.218882218C>A GRCh38
NC_000002.11:g.219746940C>A , CM000664.1:g.219746940C>A GRCh37
NC_000002.10:g.219455184C>A NCBI36
NG_012179.1:g.6686C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.171C>A MANE Select ENSP00000258411.3:p.Ala57=
ENST00000258411.7:c.171C>A ENSP00000258411.3:p.Ala57=
ENST00000458582.1:c.58C>A
NM_025216.2:c.171C>A NP_079492.2:p.Ala57=
XM_011511928.1:c.120C>A XP_011510230.1:p.Ala40=
XM_011511929.1:c.75C>A XP_011510231.1:p.Ala25=
XM_011511930.1:c.171C>A XP_011510232.1:p.Ala57=
XM_011511929.2:c.75C>A XP_011510231.1:p.Ala25=
NM_025216.3:c.171C>A MANE Select NP_079492.2:p.Ala57=
Search 100 bp 5'
Search 100 bp 3'