Canonical Allele Identifier: CA2114123
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 378862
ClinVar RCV Id: RCV000429425 RCV001232141
dbSNP Id: rs750260671
ExAC: 2:219757907 G / T
gnomAD v2: 2-219757907-G-T
gnomAD v4: 2-218893185-G-T
MyVariant Identifiers: chr2:g.219757907G>T (hg19) chr2:g.218893185G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1168G>T MANE Select ENSP00000258411.3:p.Glu390Ter
ENST00000258411.7:c.1168G>T ENSP00000258411.3:p.Glu390Ter
NM_025216.2:c.1168G>T NP_079492.2:p.Glu390Ter
XM_011511928.1:c.1117G>T XP_011510230.1:p.Glu373Ter
XM_011511929.1:c.1072G>T XP_011510231.1:p.Glu358Ter
XM_011511930.1:c.788G>T XP_011510232.1:p.Arg263Leu
XM_011511929.2:c.1072G>T XP_011510231.1:p.Glu358Ter
NM_025216.3:c.1168G>T MANE Select NP_079492.2:p.Glu390Ter
Search 100 bp 5'
Search 100 bp 3'