Canonical Allele Identifier: CA2663174556
Gene: WNT10A HGNC NCBI

Linked Data

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

HGVS Genome Assembly
NC_000002.12:g.218893201_218893206del , CM000664.2:g.218893201_218893206del GRCh38
NC_000002.11:g.219757923_219757928del , CM000664.1:g.219757923_219757928del GRCh37
NC_000002.10:g.219466167_219466172del NCBI36
NG_012179.1:g.17669_17674del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1184_1189del MANE Select ENSP00000258411.3:p.Arg395_Phe396del
ENST00000258411.7:c.1184_1189del ENSP00000258411.3:p.Arg395_Phe396del
NM_025216.2:c.1184_1189del NP_079492.2:p.Arg395_Phe396del
XM_011511928.1:c.1133_1138del XP_011510230.1:p.Arg378_Phe379del
XM_011511929.1:c.1088_1093del XP_011510231.1:p.Arg363_Phe364del
XM_011511930.1:c.804_809del XP_011510232.1:p.Leu269_Pro270del
XM_011511929.2:c.1088_1093del XP_011510231.1:p.Arg363_Phe364del
NM_025216.3:c.1184_1189del MANE Select NP_079492.2:p.Arg395_Phe396del
Search 100 bp 5'
Search 100 bp 3'