Canonical Allele Identifier: CA1328961308
Gene: WNT10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881710G= , CM000664.2:g.218881710G= GRCh38
NC_000002.11:g.219746432G= , CM000664.1:g.219746432G= GRCh37
NC_000002.10:g.219454676G= NCBI36
NG_012179.1:g.6178G=

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.114-451G= MANE Select ENSP00000258411.3:n.114-451G=
ENST00000258411.7:c.114-451G= ENSP00000258411.3:n.114-451G=
NM_025216.2:c.114-451G= NP_079492.2:n.114-451G=
XM_011511928.1:c.62+243G= XP_011510230.1:n.62+243G=
XM_011511929.1:c.18-451G= XP_011510231.1:n.18-451G=
XM_011511930.1:c.114-451G= XP_011510232.1:n.114-451G=
XM_011511929.2:c.18-451G= XP_011510231.1:n.18-451G=
NM_025216.3:c.114-451G= MANE Select NP_079492.2:n.114-451G=
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