Canonical Allele Identifier: CA350618688
Gene: WNT10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882292C>G , CM000664.2:g.218882292C>G GRCh38
NC_000002.11:g.219747014C>G , CM000664.1:g.219747014C>G GRCh37
NC_000002.10:g.219455258C>G NCBI36
NG_012179.1:g.6760C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.245C>G MANE Select ENSP00000258411.3:p.Ala82Gly
ENST00000258411.7:c.245C>G ENSP00000258411.3:p.Ala82Gly
ENST00000458582.1:c.132C>G
NM_025216.2:c.245C>G NP_079492.2:p.Ala82Gly
XM_011511928.1:c.194C>G XP_011510230.1:p.Ala65Gly
XM_011511929.1:c.149C>G XP_011510231.1:p.Ala50Gly
XM_011511930.1:c.245C>G XP_011510232.1:p.Ala82Gly
XM_011511929.2:c.149C>G XP_011510231.1:p.Ala50Gly
NM_025216.3:c.245C>G MANE Select NP_079492.2:p.Ala82Gly