Canonical Allele Identifier: CA1328961299
Gene: WNT10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881698C= , CM000664.2:g.218881698C= GRCh38
NC_000002.11:g.219746420C= , CM000664.1:g.219746420C= GRCh37
NC_000002.10:g.219454664C= NCBI36
NG_012179.1:g.6166C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.114-463C= MANE Select ENSP00000258411.3:n.114-463C=
ENST00000258411.7:c.114-463C= ENSP00000258411.3:n.114-463C=
NM_025216.2:c.114-463C= NP_079492.2:n.114-463C=
XM_011511928.1:c.62+231C= XP_011510230.1:n.62+231C=
XM_011511929.1:c.18-463C= XP_011510231.1:n.18-463C=
XM_011511930.1:c.114-463C= XP_011510232.1:n.114-463C=
XM_011511929.2:c.18-463C= XP_011510231.1:n.18-463C=
NM_025216.3:c.114-463C= MANE Select NP_079492.2:n.114-463C=
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