Canonical Allele Identifier: CA2663174557
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893243-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893244del , CM000664.2:g.218893244del GRCh38
NC_000002.11:g.219757966del , CM000664.1:g.219757966del GRCh37
NC_000002.10:g.219466210del NCBI36
NG_012179.1:g.17712del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1227del MANE Select ENSP00000258411.3:p.Thr410ProfsTer28
ENST00000258411.7:c.1227del ENSP00000258411.3:p.Thr410ProfsTer28
ENST00000489887.1:n.24del
NM_025216.2:c.1227del NP_079492.2:p.Thr410ProfsTer28
XM_011511928.1:c.1176del XP_011510230.1:p.Thr393ProfsTer28
XM_011511929.1:c.1131del XP_011510231.1:p.Thr378ProfsTer28
XM_011511930.1:c.847del XP_011510232.1:p.His283ThrfsTer9
XM_011511929.2:c.1131del XP_011510231.1:p.Thr378ProfsTer28
NM_025216.3:c.1227del MANE Select NP_079492.2:p.Thr410ProfsTer28
Search 100 bp 5'
Search 100 bp 3'