Canonical Allele Identifier: CA350592638
Gene: WNT10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893231A>C , CM000664.2:g.218893231A>C GRCh38
NC_000002.11:g.219757953A>C , CM000664.1:g.219757953A>C GRCh37
NC_000002.10:g.219466197A>C NCBI36
NG_012179.1:g.17699A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1214A>C MANE Select ENSP00000258411.3:p.Glu405Ala
ENST00000258411.7:c.1214A>C ENSP00000258411.3:p.Glu405Ala
ENST00000489887.1:n.11A>C
NM_025216.2:c.1214A>C NP_079492.2:p.Glu405Ala
XM_011511928.1:c.1163A>C XP_011510230.1:p.Glu388Ala
XM_011511929.1:c.1118A>C XP_011510231.1:p.Glu373Ala
XM_011511930.1:c.834A>C XP_011510232.1:p.Arg278=
XM_011511929.2:c.1118A>C XP_011510231.1:p.Glu373Ala
NM_025216.3:c.1214A>C MANE Select NP_079492.2:p.Glu405Ala