Canonical Allele Identifier: CA384639441
Gene: WNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981635C>A , CM000674.2:g.48981635C>A GRCh38
NC_000012.11:g.49375418C>A , CM000674.1:g.49375418C>A GRCh37
NC_000012.10:g.47661685C>A NCBI36
NG_033141.1:g.8183C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1108C>A MANE Select ENSP00000293549.3:p.Leu370Met
ENST00000293549.3:c.1108C>A ENSP00000293549.3:p.Leu370Met
ENST00000613114.4:c.1075C>A ENSP00000481240.1:p.Leu359Met
NM_005430.3:c.1108C>A NP_005421.1:p.Leu370Met
NM_005430.4:c.1108C>A MANE Select NP_005421.1:p.Leu370Met