Canonical Allele Identifier: CA431417583
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219757903C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893181C>G , CM000664.2:g.218893181C>G GRCh38
NC_000002.11:g.219757903C>G , CM000664.1:g.219757903C>G GRCh37
NC_000002.10:g.219466147C>G NCBI36
NG_012179.1:g.17649C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1164C>G MANE Select ENSP00000258411.3:p.Arg388=
ENST00000258411.7:c.1164C>G ENSP00000258411.3:p.Arg388=
NM_025216.2:c.1164C>G NP_079492.2:p.Arg388=
XM_011511928.1:c.1113C>G XP_011510230.1:p.Arg371=
XM_011511929.1:c.1068C>G XP_011510231.1:p.Arg356=
XM_011511930.1:c.784C>G XP_011510232.1:p.Gln262Glu
XM_011511929.2:c.1068C>G XP_011510231.1:p.Arg356=
NM_025216.3:c.1164C>G MANE Select NP_079492.2:p.Arg388=