Canonical Allele Identifier: CA2618600067
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981751-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981755del , CM000674.2:g.48981755del GRCh38
NC_000012.11:g.49375538del , CM000674.1:g.49375538del GRCh37
NC_000012.10:g.47661805del NCBI36
NG_033141.1:g.8303del

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*115del MANE Select ENSP00000293549.3:n.*115del
NM_005430.3:c.*115del NP_005421.1:n.*115del
NM_005430.4:c.*115del MANE Select NP_005421.1:n.*115del
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