Canonical Allele Identifier: CA2618600232
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981796-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981800del , CM000674.2:g.48981800del GRCh38
NC_000012.11:g.49375583del , CM000674.1:g.49375583del GRCh37
NC_000012.10:g.47661850del NCBI36
NG_033141.1:g.8348del

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*160del MANE Select ENSP00000293549.3:n.*160del
NM_005430.3:c.*160del NP_005421.1:n.*160del
NM_005430.4:c.*160del MANE Select NP_005421.1:n.*160del
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