Canonical Allele Identifier: CA1328965650
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1944679414
gnomAD v4: 2-218893242-ATCACC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893243_218893247del , CM000664.2:g.218893243_218893247del GRCh38
NC_000002.11:g.219757965_219757969del , CM000664.1:g.219757965_219757969del GRCh37
NC_000002.10:g.219466209_219466213del NCBI36
NG_012179.1:g.17711_17715del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1226_1230del MANE Select ENSP00000258411.3:p.Ile409ArgfsTer17
ENST00000258411.7:c.1226_1230del ENSP00000258411.3:p.Ile409ArgfsTer17
ENST00000489887.1:n.23_27del
NM_025216.2:c.1226_1230del NP_079492.2:p.Ile409ArgfsTer17
XM_011511928.1:c.1175_1179del XP_011510230.1:p.Ile392ArgfsTer17
XM_011511929.1:c.1130_1134del XP_011510231.1:p.Ile377ArgfsTer17
XM_011511930.1:c.846_850del XP_011510232.1:p.His282GlnfsTer28
XM_011511929.2:c.1130_1134del XP_011510231.1:p.Ile377ArgfsTer17
NM_025216.3:c.1226_1230del MANE Select NP_079492.2:p.Ile409ArgfsTer17
Search 100 bp 5'
Search 100 bp 3'