Canonical Allele Identifier: CA350592170
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219757907G>C (hg19) chr2:g.218893185G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893185G>C , CM000664.2:g.218893185G>C GRCh38
NC_000002.11:g.219757907G>C , CM000664.1:g.219757907G>C GRCh37
NC_000002.10:g.219466151G>C NCBI36
NG_012179.1:g.17653G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1168G>C MANE Select ENSP00000258411.3:p.Glu390Gln
ENST00000258411.7:c.1168G>C ENSP00000258411.3:p.Glu390Gln
NM_025216.2:c.1168G>C NP_079492.2:p.Glu390Gln
XM_011511928.1:c.1117G>C XP_011510230.1:p.Glu373Gln
XM_011511929.1:c.1072G>C XP_011510231.1:p.Glu358Gln
XM_011511930.1:c.788G>C XP_011510232.1:p.Arg263Pro
XM_011511929.2:c.1072G>C XP_011510231.1:p.Glu358Gln
NM_025216.3:c.1168G>C MANE Select NP_079492.2:p.Glu390Gln
Search 100 bp 5'
Search 100 bp 3'