Canonical Allele Identifier: CA350592459
Gene: WNT10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893210G>C , CM000664.2:g.218893210G>C GRCh38
NC_000002.11:g.219757932G>C , CM000664.1:g.219757932G>C GRCh37
NC_000002.10:g.219466176G>C NCBI36
NG_012179.1:g.17678G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1193G>C MANE Select ENSP00000258411.3:p.Trp398Ser
ENST00000258411.7:c.1193G>C ENSP00000258411.3:p.Trp398Ser
NM_025216.2:c.1193G>C NP_079492.2:p.Trp398Ser
XM_011511928.1:c.1142G>C XP_011510230.1:p.Trp381Ser
XM_011511929.1:c.1097G>C XP_011510231.1:p.Trp366Ser
XM_011511930.1:c.813G>C XP_011510232.1:p.Leu271=
XM_011511929.2:c.1097G>C XP_011510231.1:p.Trp366Ser
NM_025216.3:c.1193G>C MANE Select NP_079492.2:p.Trp398Ser