Canonical Allele Identifier: CA1328965797
Gene: WNT10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893388A= , CM000664.2:g.218893388A= GRCh38
NC_000002.11:g.219758110A= , CM000664.1:g.219758110A= GRCh37
NC_000002.10:g.219466354A= NCBI36
NG_012179.1:g.17856A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.*117A= MANE Select ENSP00000258411.3:n.*117A=
ENST00000258411.7:c.*117A= ENSP00000258411.3:n.*117A=
ENST00000489887.1:n.47+121A=
NM_025216.2:c.*117A= NP_079492.2:n.*117A=
XM_011511928.1:c.*117A= XP_011510230.1:n.*117A=
XM_011511929.1:c.*117A= XP_011510231.1:n.*117A=
XM_011511930.1:c.*91A= XP_011510232.1:n.*91A=
XM_011511929.2:c.*117A= XP_011510231.1:n.*117A=
NM_025216.3:c.*117A= MANE Select NP_079492.2:n.*117A=
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