Canonical Allele Identifier: CA2663174656
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893349-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893349G>A , CM000664.2:g.218893349G>A GRCh38
NC_000002.11:g.219758071G>A , CM000664.1:g.219758071G>A GRCh37
NC_000002.10:g.219466315G>A NCBI36
NG_012179.1:g.17817G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.*78G>A MANE Select ENSP00000258411.3:n.*78G>A
ENST00000258411.7:c.*78G>A ENSP00000258411.3:n.*78G>A
ENST00000489887.1:n.47+82G>A
NM_025216.2:c.*78G>A NP_079492.2:n.*78G>A
XM_011511928.1:c.*78G>A XP_011510230.1:n.*78G>A
XM_011511929.1:c.*78G>A XP_011510231.1:n.*78G>A
XM_011511930.1:c.*52G>A XP_011510232.1:n.*52G>A
XM_011511929.2:c.*78G>A XP_011510231.1:n.*78G>A
NM_025216.3:c.*78G>A MANE Select NP_079492.2:n.*78G>A
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