Canonical Allele Identifier: CA350592599
Gene: WNT10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893227T>G , CM000664.2:g.218893227T>G GRCh38
NC_000002.11:g.219757949T>G , CM000664.1:g.219757949T>G GRCh37
NC_000002.10:g.219466193T>G NCBI36
NG_012179.1:g.17695T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1210T>G MANE Select ENSP00000258411.3:p.Cys404Gly
ENST00000258411.7:c.1210T>G ENSP00000258411.3:p.Cys404Gly
ENST00000489887.1:n.7T>G
NM_025216.2:c.1210T>G NP_079492.2:p.Cys404Gly
XM_011511928.1:c.1159T>G XP_011510230.1:p.Cys387Gly
XM_011511929.1:c.1114T>G XP_011510231.1:p.Cys372Gly
XM_011511930.1:c.830T>G XP_011510232.1:p.Leu277Arg
XM_011511929.2:c.1114T>G XP_011510231.1:p.Cys372Gly
NM_025216.3:c.1210T>G MANE Select NP_079492.2:p.Cys404Gly