Canonical Allele Identifier: CA2618599795
Gene: WNT1 HGNC NCBI

Linked Data

gnomAD v4: 12-48981657-GC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981662del , CM000674.2:g.48981662del GRCh38
NC_000012.11:g.49375445del , CM000674.1:g.49375445del GRCh37
NC_000012.10:g.47661712del NCBI36
NG_033141.1:g.8210del

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*22del MANE Select ENSP00000293549.3:n.*22del
ENST00000293549.3:c.*22del ENSP00000293549.3:n.*22del
NM_005430.3:c.*22del NP_005421.1:n.*22del
NM_005430.4:c.*22del MANE Select NP_005421.1:n.*22del
Search 100 bp 5'
Search 100 bp 3'