Canonical Allele Identifier: CA1328961311
Gene: WNT10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881712C= , CM000664.2:g.218881712C= GRCh38
NC_000002.11:g.219746434C= , CM000664.1:g.219746434C= GRCh37
NC_000002.10:g.219454678C= NCBI36
NG_012179.1:g.6180C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.114-449C= MANE Select ENSP00000258411.3:n.114-449C=
ENST00000258411.7:c.114-449C= ENSP00000258411.3:n.114-449C=
NM_025216.2:c.114-449C= NP_079492.2:n.114-449C=
XM_011511928.1:c.62+245C= XP_011510230.1:n.62+245C=
XM_011511929.1:c.18-449C= XP_011510231.1:n.18-449C=
XM_011511930.1:c.114-449C= XP_011510232.1:n.114-449C=
XM_011511929.2:c.18-449C= XP_011510231.1:n.18-449C=
NM_025216.3:c.114-449C= MANE Select NP_079492.2:n.114-449C=
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