Canonical Allele Identifier: CA350592742
Gene: WNT10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893243T>C , CM000664.2:g.218893243T>C GRCh38
NC_000002.11:g.219757965T>C , CM000664.1:g.219757965T>C GRCh37
NC_000002.10:g.219466209T>C NCBI36
NG_012179.1:g.17711T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1226T>C MANE Select ENSP00000258411.3:p.Ile409Thr
ENST00000258411.7:c.1226T>C ENSP00000258411.3:p.Ile409Thr
ENST00000489887.1:n.23T>C
NM_025216.2:c.1226T>C NP_079492.2:p.Ile409Thr
XM_011511928.1:c.1175T>C XP_011510230.1:p.Ile392Thr
XM_011511929.1:c.1130T>C XP_011510231.1:p.Ile377Thr
XM_011511930.1:c.846T>C XP_011510232.1:p.His282=
XM_011511929.2:c.1130T>C XP_011510231.1:p.Ile377Thr
NM_025216.3:c.1226T>C MANE Select NP_079492.2:p.Ile409Thr