Canonical Allele Identifier: CA350592415
Gene: WNT10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893208C>A , CM000664.2:g.218893208C>A GRCh38
NC_000002.11:g.219757930C>A , CM000664.1:g.219757930C>A GRCh37
NC_000002.10:g.219466174C>A NCBI36
NG_012179.1:g.17676C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1191C>A MANE Select ENSP00000258411.3:p.His397Gln
ENST00000258411.7:c.1191C>A ENSP00000258411.3:p.His397Gln
NM_025216.2:c.1191C>A NP_079492.2:p.His397Gln
XM_011511928.1:c.1140C>A XP_011510230.1:p.His380Gln
XM_011511929.1:c.1095C>A XP_011510231.1:p.His365Gln
XM_011511930.1:c.811C>A XP_011510232.1:p.Leu271Met
XM_011511929.2:c.1095C>A XP_011510231.1:p.His365Gln
NM_025216.3:c.1191C>A MANE Select NP_079492.2:p.His397Gln