Canonical Allele Identifier: CA350592571
Gene: WNT10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893225T>A , CM000664.2:g.218893225T>A GRCh38
NC_000002.11:g.219757947T>A , CM000664.1:g.219757947T>A GRCh37
NC_000002.10:g.219466191T>A NCBI36
NG_012179.1:g.17693T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1208T>A MANE Select ENSP00000258411.3:p.Val403Asp
ENST00000258411.7:c.1208T>A ENSP00000258411.3:p.Val403Asp
ENST00000489887.1:n.5T>A
NM_025216.2:c.1208T>A NP_079492.2:p.Val403Asp
XM_011511928.1:c.1157T>A XP_011510230.1:p.Val386Asp
XM_011511929.1:c.1112T>A XP_011510231.1:p.Val371Asp
XM_011511930.1:c.828T>A XP_011510232.1:p.Gly276=
XM_011511929.2:c.1112T>A XP_011510231.1:p.Val371Asp
NM_025216.3:c.1208T>A MANE Select NP_079492.2:p.Val403Asp