Canonical Allele Identifier: CA2663174292
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218890264-CTTCGGGGAGCGCTT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218890268_218890281del , CM000664.2:g.218890268_218890281del GRCh38
NC_000002.11:g.219754990_219755003del , CM000664.1:g.219754990_219755003del GRCh37
NC_000002.10:g.219463234_219463247del NCBI36
NG_012179.1:g.14736_14749del

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.661_674del MANE Select ENSP00000258411.3:p.Gly221Ter
ENST00000258411.7:c.661_674del ENSP00000258411.3:p.Gly221Ter
ENST00000458582.1:c.264-2506_264-2493del
NM_025216.2:c.661_674del NP_079492.2:p.Gly221Ter
XM_011511928.1:c.610_623del XP_011510230.1:p.Gly204Ter
XM_011511929.1:c.565_578del XP_011510231.1:p.Gly189Ter
XM_011511930.1:c.377-2506_377-2493del XP_011510232.1:n.377-2506_377-2493del
XM_011511929.2:c.565_578del XP_011510231.1:p.Gly189Ter
NM_025216.3:c.661_674del MANE Select NP_079492.2:p.Gly221Ter
Search 100 bp 5'
Search 100 bp 3'