Canonical Allele Identifier: CA2663174558
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893265-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893267del , CM000664.2:g.218893267del GRCh38
NC_000002.11:g.219757989del , CM000664.1:g.219757989del GRCh37
NC_000002.10:g.219466233del NCBI36
NG_012179.1:g.17735del

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.1250del MANE Select ENSP00000258411.3:p.Lys417SerfsTer21
ENST00000258411.7:c.1250del ENSP00000258411.3:p.Lys417SerfsTer21
ENST00000489887.1:n.47del
NM_025216.2:c.1250del NP_079492.2:p.Lys417SerfsTer21
XM_011511928.1:c.1199del XP_011510230.1:p.Lys400SerfsTer21
XM_011511929.1:c.1154del XP_011510231.1:p.Lys385SerfsTer21
XM_011511930.1:c.870del XP_011510232.1:p.Val291Ter
XM_011511929.2:c.1154del XP_011510231.1:p.Lys385SerfsTer21
NM_025216.3:c.1250del MANE Select NP_079492.2:p.Lys417SerfsTer21
Search 100 bp 5'
Search 100 bp 3'