Canonical Allele Identifier: CA1328965822
Gene: WNT10A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893410C= , CM000664.2:g.218893410C= GRCh38
NC_000002.11:g.219758132C= , CM000664.1:g.219758132C= GRCh37
NC_000002.10:g.219466376C= NCBI36
NG_012179.1:g.17878C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.*139C= MANE Select ENSP00000258411.3:n.*139C=
ENST00000258411.7:c.*139C= ENSP00000258411.3:n.*139C=
ENST00000489887.1:n.47+143C=
NM_025216.2:c.*139C= NP_079492.2:n.*139C=
XM_011511928.1:c.*139C= XP_011510230.1:n.*139C=
XM_011511929.1:c.*139C= XP_011510231.1:n.*139C=
XM_011511930.1:c.*113C= XP_011510232.1:n.*113C=
XM_011511929.2:c.*139C= XP_011510231.1:n.*139C=
NM_025216.3:c.*139C= MANE Select NP_079492.2:n.*139C=
Search 100 bp 5'
Search 100 bp 3'