Canonical Allele Identifier: CA2034902135
Gene: WNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981651G= , CM000674.2:g.48981651G= GRCh38
NC_000012.11:g.49375434G= , CM000674.1:g.49375434G= GRCh37
NC_000012.10:g.47661701G= NCBI36
NG_033141.1:g.8199G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*11G= MANE Select ENSP00000293549.3:n.*11G=
ENST00000293549.3:c.*11G= ENSP00000293549.3:n.*11G=
NM_005430.3:c.*11G= NP_005421.1:n.*11G=
NM_005430.4:c.*11G= MANE Select NP_005421.1:n.*11G=