Canonical Allele Identifier: CA1328961304
Gene: WNT10A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881704G= , CM000664.2:g.218881704G= GRCh38
NC_000002.11:g.219746426G= , CM000664.1:g.219746426G= GRCh37
NC_000002.10:g.219454670G= NCBI36
NG_012179.1:g.6172G=

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.114-457G= MANE Select ENSP00000258411.3:n.114-457G=
ENST00000258411.7:c.114-457G= ENSP00000258411.3:n.114-457G=
NM_025216.2:c.114-457G= NP_079492.2:n.114-457G=
XM_011511928.1:c.62+237G= XP_011510230.1:n.62+237G=
XM_011511929.1:c.18-457G= XP_011510231.1:n.18-457G=
XM_011511930.1:c.114-457G= XP_011510232.1:n.114-457G=
XM_011511929.2:c.18-457G= XP_011510231.1:n.18-457G=
NM_025216.3:c.114-457G= MANE Select NP_079492.2:n.114-457G=
Search 100 bp 5'
Search 100 bp 3'