Canonical Allele Identifier: CA2663174675
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893373-AGAG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893377_218893379del , CM000664.2:g.218893377_218893379del GRCh38
NC_000002.11:g.219758099_219758101del , CM000664.1:g.219758099_219758101del GRCh37
NC_000002.10:g.219466343_219466345del NCBI36
NG_012179.1:g.17845_17847del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.*106_*108del MANE Select ENSP00000258411.3:n.*106_*108del
ENST00000258411.7:c.*106_*108del ENSP00000258411.3:n.*106_*108del
ENST00000489887.1:n.47+110_47+112del
NM_025216.2:c.*106_*108del NP_079492.2:n.*106_*108del
XM_011511928.1:c.*106_*108del XP_011510230.1:n.*106_*108del
XM_011511929.1:c.*106_*108del XP_011510231.1:n.*106_*108del
XM_011511930.1:c.*80_*82del XP_011510232.1:n.*80_*82del
XM_011511929.2:c.*106_*108del XP_011510231.1:n.*106_*108del
NM_025216.3:c.*106_*108del MANE Select NP_079492.2:n.*106_*108del
Search 100 bp 5'
Search 100 bp 3'