Canonical Allele Identifier: CA2034902151
Gene: WNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981675C= , CM000674.2:g.48981675C= GRCh38
NC_000012.11:g.49375458C= , CM000674.1:g.49375458C= GRCh37
NC_000012.10:g.47661725C= NCBI36
NG_033141.1:g.8223C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*35C= MANE Select ENSP00000293549.3:n.*35C=
ENST00000293549.3:c.*35C= ENSP00000293549.3:n.*35C=
NM_005430.3:c.*35C= NP_005421.1:n.*35C=
NM_005430.4:c.*35C= MANE Select NP_005421.1:n.*35C=