Canonical Allele Identifier: CA1328961477
Gene: WNT10A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882105T= , CM000664.2:g.218882105T= GRCh38
NC_000002.11:g.219746827T= , CM000664.1:g.219746827T= GRCh37
NC_000002.10:g.219455071T= NCBI36
NG_012179.1:g.6573T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-56T= MANE Select ENSP00000258411.3:n.114-56T=
ENST00000258411.7:c.114-56T= ENSP00000258411.3:n.114-56T=
NM_025216.2:c.114-56T= NP_079492.2:n.114-56T=
XM_011511928.1:c.63-56T= XP_011510230.1:n.63-56T=
XM_011511929.1:c.18-56T= XP_011510231.1:n.18-56T=
XM_011511930.1:c.114-56T= XP_011510232.1:n.114-56T=
XM_011511929.2:c.18-56T= XP_011510231.1:n.18-56T=
NM_025216.3:c.114-56T= MANE Select NP_079492.2:n.114-56T=
Search 100 bp 5'
Search 100 bp 3'