Canonical Allele Identifier: CA2663174559
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893272-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893272G>T , CM000664.2:g.218893272G>T GRCh38
NC_000002.11:g.219757994G>T , CM000664.1:g.219757994G>T GRCh37
NC_000002.10:g.219466238G>T NCBI36
NG_012179.1:g.17740G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.*1G>T MANE Select ENSP00000258411.3:n.*1G>T
ENST00000258411.7:c.*1G>T ENSP00000258411.3:n.*1G>T
ENST00000489887.1:n.47+5G>T
NM_025216.2:c.*1G>T NP_079492.2:n.*1G>T
XM_011511928.1:c.*1G>T XP_011510230.1:n.*1G>T
XM_011511929.1:c.*1G>T XP_011510231.1:n.*1G>T
XM_011511930.1:c.875G>T XP_011510232.1:p.Ser292Ile
XM_011511929.2:c.*1G>T XP_011510231.1:n.*1G>T
NM_025216.3:c.*1G>T MANE Select NP_079492.2:n.*1G>T
Search 100 bp 5'
Search 100 bp 3'