Canonical Allele Identifier: CA431416465
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219746982G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882260G>A , CM000664.2:g.218882260G>A GRCh38
NC_000002.11:g.219746982G>A , CM000664.1:g.219746982G>A GRCh37
NC_000002.10:g.219455226G>A NCBI36
NG_012179.1:g.6728G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.213G>A MANE Select ENSP00000258411.3:p.Gln71=
ENST00000258411.7:c.213G>A ENSP00000258411.3:p.Gln71=
ENST00000458582.1:c.100G>A
NM_025216.2:c.213G>A NP_079492.2:p.Gln71=
XM_011511928.1:c.162G>A XP_011510230.1:p.Gln54=
XM_011511929.1:c.117G>A XP_011510231.1:p.Gln39=
XM_011511930.1:c.213G>A XP_011510232.1:p.Gln71=
XM_011511929.2:c.117G>A XP_011510231.1:p.Gln39=
NM_025216.3:c.213G>A MANE Select NP_079492.2:p.Gln71=
Search 100 bp 5'
Search 100 bp 3'