Canonical Allele Identifier: CA1328965769
Gene: WNT10A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893374G= , CM000664.2:g.218893374G= GRCh38
NC_000002.11:g.219758096G= , CM000664.1:g.219758096G= GRCh37
NC_000002.10:g.219466340G= NCBI36
NG_012179.1:g.17842G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.*103G= MANE Select ENSP00000258411.3:n.*103G=
ENST00000258411.7:c.*103G= ENSP00000258411.3:n.*103G=
ENST00000489887.1:n.47+107G=
NM_025216.2:c.*103G= NP_079492.2:n.*103G=
XM_011511928.1:c.*103G= XP_011510230.1:n.*103G=
XM_011511929.1:c.*103G= XP_011510231.1:n.*103G=
XM_011511930.1:c.*77G= XP_011510232.1:n.*77G=
XM_011511929.2:c.*103G= XP_011510231.1:n.*103G=
NM_025216.3:c.*103G= MANE Select NP_079492.2:n.*103G=
Search 100 bp 5'
Search 100 bp 3'