Canonical Allele Identifier: CA116865
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 4461
dbSNP Id: rs121908119

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882368C>A , CM000664.2:g.218882368C>A GRCh38
NC_000002.11:g.219747090C>A , CM000664.1:g.219747090C>A GRCh37
NC_000002.10:g.219455334C>A NCBI36
NG_012179.1:g.6836C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.321C>A MANE Select ENSP00000258411.3:p.Cys107Ter
ENST00000258411.7:c.321C>A ENSP00000258411.3:p.Cys107Ter
ENST00000458582.1:c.208C>A
NM_025216.2:c.321C>A NP_079492.2:p.Cys107Ter
XM_011511928.1:c.270C>A XP_011510230.1:p.Cys90Ter
XM_011511929.1:c.225C>A XP_011510231.1:p.Cys75Ter
XM_011511930.1:c.321C>A XP_011510232.1:p.Cys107Ter
XM_011511929.2:c.225C>A XP_011510231.1:p.Cys75Ter
NM_025216.3:c.321C>A MANE Select NP_079492.2:p.Cys107Ter