Canonical Allele Identifier: CA1328965831
Gene: WNT10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893415C= , CM000664.2:g.218893415C= GRCh38
NC_000002.11:g.219758137C= , CM000664.1:g.219758137C= GRCh37
NC_000002.10:g.219466381C= NCBI36
NG_012179.1:g.17883C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.*144C= MANE Select ENSP00000258411.3:n.*144C=
ENST00000258411.7:c.*144C= ENSP00000258411.3:n.*144C=
ENST00000489887.1:n.47+148C=
NM_025216.2:c.*144C= NP_079492.2:n.*144C=
XM_011511928.1:c.*144C= XP_011510230.1:n.*144C=
XM_011511929.1:c.*144C= XP_011510231.1:n.*144C=
XM_011511930.1:c.*118C= XP_011510232.1:n.*118C=
XM_011511929.2:c.*144C= XP_011510231.1:n.*144C=
NM_025216.3:c.*144C= MANE Select NP_079492.2:n.*144C=
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