Canonical Allele Identifier: CA654731922
Gene: WNT10B HGNC NCBI

Linked Data

COSMIC: COSN24911201
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48965918del , CM000674.2:g.48965918del GRCh38
NC_000012.11:g.49359701del , CM000674.1:g.49359701del GRCh37
NC_000012.10:g.47645968del NCBI36
NG_023347.1:g.10944del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301061.9:c.*180del MANE Select ENSP00000301061.4:n.*180del
ENST00000301061.8:c.*180del ENSP00000301061.4:n.*180del
ENST00000403957.5:c.*632del ENSP00000385980.1:n.*632del
ENST00000407467.5:c.*632del ENSP00000384691.1:n.*632del
NM_003394.3:c.*180del NP_003385.2:n.*180del
XM_011538721.1:c.*180del XP_011537023.1:n.*180del
XM_011538722.1:c.*180del XP_011537024.1:n.*180del
XM_017019919.1:c.*180del XP_016875408.1:n.*180del
XM_024449179.1:c.*180del XP_024304947.1:n.*180del
NM_003394.4:c.*180del MANE Select NP_003385.2:n.*180del
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