Canonical Allele Identifier: CA2034902138
Gene: WNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981656C= , CM000674.2:g.48981656C= GRCh38
NC_000012.11:g.49375439C= , CM000674.1:g.49375439C= GRCh37
NC_000012.10:g.47661706C= NCBI36
NG_033141.1:g.8204C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*16C= MANE Select ENSP00000293549.3:n.*16C=
ENST00000293549.3:c.*16C= ENSP00000293549.3:n.*16C=
NM_005430.3:c.*16C= NP_005421.1:n.*16C=
NM_005430.4:c.*16C= MANE Select NP_005421.1:n.*16C=