Canonical Allele Identifier: CA2663174291
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218890246-CTGCAGCCCCGACA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218890249_218890261del , CM000664.2:g.218890249_218890261del GRCh38
NC_000002.11:g.219754971_219754983del , CM000664.1:g.219754971_219754983del GRCh37
NC_000002.10:g.219463215_219463227del NCBI36
NG_012179.1:g.14717_14729del

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.642_654del MANE Select ENSP00000258411.3:p.Cys214TrpfsTer25
ENST00000258411.7:c.642_654del ENSP00000258411.3:p.Cys214TrpfsTer25
ENST00000458582.1:c.264-2525_264-2513del
NM_025216.2:c.642_654del NP_079492.2:p.Cys214TrpfsTer25
XM_011511928.1:c.591_603del XP_011510230.1:p.Cys197TrpfsTer25
XM_011511929.1:c.546_558del XP_011510231.1:p.Cys182TrpfsTer25
XM_011511930.1:c.377-2525_377-2513del XP_011510232.1:n.377-2525_377-2513del
XM_011511929.2:c.546_558del XP_011510231.1:p.Cys182TrpfsTer25
NM_025216.3:c.642_654del MANE Select NP_079492.2:p.Cys214TrpfsTer25
Search 100 bp 5'
Search 100 bp 3'