Canonical Allele Identifier: CA350592657
Gene: WNT10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893232A>C , CM000664.2:g.218893232A>C GRCh38
NC_000002.11:g.219757954A>C , CM000664.1:g.219757954A>C GRCh37
NC_000002.10:g.219466198A>C NCBI36
NG_012179.1:g.17700A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1215A>C MANE Select ENSP00000258411.3:p.Glu405Asp
ENST00000258411.7:c.1215A>C ENSP00000258411.3:p.Glu405Asp
ENST00000489887.1:n.12A>C
NM_025216.2:c.1215A>C NP_079492.2:p.Glu405Asp
XM_011511928.1:c.1164A>C XP_011510230.1:p.Glu388Asp
XM_011511929.1:c.1119A>C XP_011510231.1:p.Glu373Asp
XM_011511930.1:c.835A>C XP_011510232.1:p.Arg279=
XM_011511929.2:c.1119A>C XP_011510231.1:p.Glu373Asp
NM_025216.3:c.1215A>C MANE Select NP_079492.2:p.Glu405Asp