Canonical Allele Identifier: CA2034902152
Gene: WNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981676T= , CM000674.2:g.48981676T= GRCh38
NC_000012.11:g.49375459T= , CM000674.1:g.49375459T= GRCh37
NC_000012.10:g.47661726T= NCBI36
NG_033141.1:g.8224T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*36T= MANE Select ENSP00000293549.3:n.*36T=
ENST00000293549.3:c.*36T= ENSP00000293549.3:n.*36T=
NM_005430.3:c.*36T= NP_005421.1:n.*36T=
NM_005430.4:c.*36T= MANE Select NP_005421.1:n.*36T=