Canonical Allele Identifier: CA2663174555
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893198-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893200del , CM000664.2:g.218893200del GRCh38
NC_000002.11:g.219757922del , CM000664.1:g.219757922del GRCh37
NC_000002.10:g.219466166del NCBI36
NG_012179.1:g.17668del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1183del MANE Select ENSP00000258411.3:p.Arg395AlafsTer?
ENST00000258411.7:c.1183del ENSP00000258411.3:p.Arg395AlafsTer?
NM_025216.2:c.1183del NP_079492.2:p.Arg395AlafsTer?
XM_011511928.1:c.1132del XP_011510230.1:p.Arg378AlafsTer?
XM_011511929.1:c.1087del XP_011510231.1:p.Arg363AlafsTer?
XM_011511930.1:c.803del XP_011510232.1:p.Pro268ArgfsTer24
XM_011511929.2:c.1087del XP_011510231.1:p.Arg363AlafsTer?
NM_025216.3:c.1183del MANE Select NP_079492.2:p.Arg395AlafsTer?
Search 100 bp 5'
Search 100 bp 3'