Canonical Allele Identifier: CA350592778
Gene: WNT10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893251T>C , CM000664.2:g.218893251T>C GRCh38
NC_000002.11:g.219757973T>C , CM000664.1:g.219757973T>C GRCh37
NC_000002.10:g.219466217T>C NCBI36
NG_012179.1:g.17719T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1234T>C MANE Select ENSP00000258411.3:p.Trp412Arg
ENST00000258411.7:c.1234T>C ENSP00000258411.3:p.Trp412Arg
ENST00000489887.1:n.31T>C
NM_025216.2:c.1234T>C NP_079492.2:p.Trp412Arg
XM_011511928.1:c.1183T>C XP_011510230.1:p.Trp395Arg
XM_011511929.1:c.1138T>C XP_011510231.1:p.Trp380Arg
XM_011511930.1:c.854T>C XP_011510232.1:p.Val285Ala
XM_011511929.2:c.1138T>C XP_011510231.1:p.Trp380Arg
NM_025216.3:c.1234T>C MANE Select NP_079492.2:p.Trp412Arg