Canonical Allele Identifier: CA431234853
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219757963C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893241C>G , CM000664.2:g.218893241C>G GRCh38
NC_000002.11:g.219757963C>G , CM000664.1:g.219757963C>G GRCh37
NC_000002.10:g.219466207C>G NCBI36
NG_012179.1:g.17709C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1224C>G MANE Select ENSP00000258411.3:p.Arg408=
ENST00000258411.7:c.1224C>G ENSP00000258411.3:p.Arg408=
ENST00000489887.1:n.21C>G
NM_025216.2:c.1224C>G NP_079492.2:p.Arg408=
XM_011511928.1:c.1173C>G XP_011510230.1:p.Arg391=
XM_011511929.1:c.1128C>G XP_011510231.1:p.Arg376=
XM_011511930.1:c.844C>G XP_011510232.1:p.His282Asp
XM_011511929.2:c.1128C>G XP_011510231.1:p.Arg376=
NM_025216.3:c.1224C>G MANE Select NP_079492.2:p.Arg408=