Canonical Allele Identifier: CA2663174701
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893406-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893406C>T , CM000664.2:g.218893406C>T GRCh38
NC_000002.11:g.219758128C>T , CM000664.1:g.219758128C>T GRCh37
NC_000002.10:g.219466372C>T NCBI36
NG_012179.1:g.17874C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.*135C>T MANE Select ENSP00000258411.3:n.*135C>T
ENST00000258411.7:c.*135C>T ENSP00000258411.3:n.*135C>T
ENST00000489887.1:n.47+139C>T
NM_025216.2:c.*135C>T NP_079492.2:n.*135C>T
XM_011511928.1:c.*135C>T XP_011510230.1:n.*135C>T
XM_011511929.1:c.*135C>T XP_011510231.1:n.*135C>T
XM_011511930.1:c.*109C>T XP_011510232.1:n.*109C>T
XM_011511929.2:c.*135C>T XP_011510231.1:n.*135C>T
NM_025216.3:c.*135C>T MANE Select NP_079492.2:n.*135C>T
Search 100 bp 5'
Search 100 bp 3'