Canonical Allele Identifier: CA431416484
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs2106011617
MyVariant Identifiers: chr2:g.219747015T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882293T>A , CM000664.2:g.218882293T>A GRCh38
NC_000002.11:g.219747015T>A , CM000664.1:g.219747015T>A GRCh37
NC_000002.10:g.219455259T>A NCBI36
NG_012179.1:g.6761T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.246T>A MANE Select ENSP00000258411.3:p.Ala82=
ENST00000258411.7:c.246T>A ENSP00000258411.3:p.Ala82=
ENST00000458582.1:c.133T>A
NM_025216.2:c.246T>A NP_079492.2:p.Ala82=
XM_011511928.1:c.195T>A XP_011510230.1:p.Ala65=
XM_011511929.1:c.150T>A XP_011510231.1:p.Ala50=
XM_011511930.1:c.246T>A XP_011510232.1:p.Ala82=
XM_011511929.2:c.150T>A XP_011510231.1:p.Ala50=
NM_025216.3:c.246T>A MANE Select NP_079492.2:p.Ala82=
Search 100 bp 5'
Search 100 bp 3'